FDA Class II · Medical device · June 17, 2026
Brand Name recall — HF Acquisition Co LLC
Due to incorrect incubation process being performed on product.
Company / brand: HF Acquisition Co recalls
Official ID Z-2331-2026 · Official record ↗
FDA recalls — page 7
2,784 recent recalls from the U.S. Food & Drug Administration in our current data (last 90 days). Showing 1,801–2,100, newest first.
FDA Class II · Medical device · June 17, 2026
CGuard¿ Prime Carotid Stent System recall — INSPIREMD Inc
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Official ID Z-2330-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
CGuard Prime Carotid Stent System recall — INSPIREMD Inc
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Official ID Z-2329-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Brand Name recall — INSPIREMD Inc
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Official ID Z-2328-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
CGuard Prime Carotid Stent System recall — INSPIREMD Inc
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Official ID Z-2327-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Brand Name recall — INSPIREMD Inc
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Official ID Z-2326-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Brand Name recall — INSPIREMD Inc
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Official ID Z-2325-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
TDC VELOCE" recall — D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls
Official ID Z-2324-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
TDC VELOCE" recall — D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls
Official ID Z-2323-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
TDC VELOCE" recall — D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls
Official ID Z-2322-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Bicarby" Dialysate recall — Fresenius Medical Care Holdings, Inc.
Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-…
Company / brand: Fresenius Medical Care Holdings recalls
Official ID Z-2321-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves recall — BERLIN HEART GMBH
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
Company / brand: BERLIN HEART recalls
Official ID Z-2320-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Mahurkar Elite PASS Trays recall — Mozarc Medical US LLC
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.
Company / brand: Mozarc Medical US recalls
Official ID Z-2319-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Allia Moveo angiographic X-ray system recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Official ID Z-2318-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Allia IGS Pulse angiographic X-ray system recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Official ID Z-2317-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Allia IGS 7 Pulse angiographic X-ray system recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Official ID Z-2316-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Allia IGS 5 Pulse angiographic X-ray system recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Official ID Z-2315-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Allia IGS 3 Pulse angiographic X-ray system recall — GE Medical Systems, LLC
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Official ID Z-2314-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Plum Duo Precision IV Pump recall — ICU Medical, Inc.
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Company / brand: ICU Medical recalls
Official ID Z-2313-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Plum Duo Infusion Pump recall — ICU Medical, Inc.
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Company / brand: ICU Medical recalls
Official ID Z-2312-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Plum Solo Precision IV Pump recall — ICU Medical, Inc.
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Company / brand: ICU Medical recalls
Official ID Z-2311-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Fresh Roast Systems ColorTrack recall — Fresh Roast Systems Inc
A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific misuse circumstances …
Company / brand: Fresh Roast Systems recalls
Official ID Z-2280-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
NEURO NOURISH dietary supplement recall — SENSORY SUPPLEMENT LLC
Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
Company / brand: SENSORY SUPPLEMENT recalls
Official ID H-1109-2026 · Official record ↗
FDA Class I · Food · June 17, 2026
Taro Cakes UPC CODE #652565100055 recall — E & S Grocery & Bakery Inc.
Undeclared Egg Allergen
Company / brand: E & S Grocery & Bakery recalls
Official ID H-0944-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
DRAGONFLY Thai Ginger Powder Net Weight recall — U.S. Tov, Inc. dba U.S. Trading Company
Potential contamination with lead.
Company / brand: U.S. Tov recalls
Official ID H-0943-2026 · Official record ↗
FDA Class I · Food · June 17, 2026
1 recall — Total Nutrition Inc
Product may be contaminated with Salmonella.
Company / brand: Total Nutrition recalls
Official ID H-0942-2026 · Official record ↗
FDA Class I · Food · June 17, 2026
Individual Unit Label (both lid and front of cup) recall — Kettle Cuisine, LLC
Contains undeclared allergen (shrimp).
Company / brand: Kettle Cuisine recalls
Official ID H-0941-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Park St recall — BEF Foods, Inc
Undeclared allergen (soy lecithin).
Company / brand: BEF Foods recalls
Official ID H-0940-2026 · Official record ↗
FDA Class I · Food · June 17, 2026
HH Fresh Trading Corp recall — HH FRESH TRADING CORP
Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.
Company / brand: HH FRESH TRADING recalls
Official ID H-0939-2026 · Official record ↗
FDA Class III · Food · June 17, 2026
MMB of Louisiana Pasteurized Donor Human Milk recall — Mothers' Milk Bank of Louisiana at Ochsner Baptist
Potential physical contamination: dark spot was noticed on the bottom of container.
Company / brand: Mothers' Milk Bank of Louisiana at Ochsner Baptist recalls
Official ID H-0938-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Flan Cake [image] Custard Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0937-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cheesecake de Guava [image] Guava Cheesecake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0936-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cheesecake de Fresa [image] Strawberry Cheesecake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0935-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cheesecake de Mango [image] Mango Cheesecake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0934-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cheesecake de Dulce de Leche [image] Caramel Cheesecake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0933-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Marquesita de Chocolate y Vainilla [image] Delighted Flavored Cakes The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0932-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Marquesita de Dulceleche [image] Delighted Flavored Cakes The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0931-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Marquesita de Fresa [image] Delighted Flavored Cakes The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0930-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Marquesita de Mango [image] Delighted Flavored Cakes The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0929-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Marquesita de Guava [image] Delighted Flavored Cakes The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0928-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Tiramisu [image] Cofee Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0927-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cake de Mango [image] Mango Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0926-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cake de Guayaba [image] Guava Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0925-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cake de Fresa y Chocolate [image] Stawberry & Chocolate Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0924-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cake de Coco [image] Coconut Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0923-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Cake de Capuchino [image] Capuchino Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0922-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Capuchino [image] Syrup Cone Cake The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0921-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Rollitos de DulceLeche [image] Caramel Rolls The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0920-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Rollitos de Guava [image] Guava Rolls The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0919-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Jumbo Napolitano [image] Jumbo Neapolitan recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0918-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Napolitano [image] Neapolitan The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0917-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Jumbo Brazo Gitano Caramelo [image] Jumbo Caramel Roll The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0916-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Brazo Gitano [image] Caramel Sweet Roll The Original recall — Galaxy RG Corp
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Company / brand: Galaxy RG recalls
Official ID H-0915-2026 · Official record ↗
FDA Class III · Food · June 17, 2026
ESTRELLA recall — Refresqueria Estrella Inc.
Undeclared FD&C Red 40
Company / brand: Refresqueria Estrella recalls
Official ID H-0913-2026 · Official record ↗
FDA Class II · Food · June 17, 2026
Farm Rich Pizza Cheese Crunchers recall — Rich Products Corp
May contain metal pieces
Company / brand: Rich Products recalls
Official ID H-0912-2026 · Official record ↗
FDA Class III · Food · June 17, 2026
WeiKFiELD Custard Powder Kesar Pista recall — Weikfield Foods Pvt. Ltd.
The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.
Company / brand: Weikfield Foods recalls
Official ID H-0911-2026 · Official record ↗
FDA Class I · Drug · June 17, 2026
BEEKEEPER'S NATURALS Saline Nasal Spray recall — BEEKEEPER'S NATURALS USA INC.
Microbial Contamination of Non-Sterile Products
Company / brand: BEEKEEPER'S NATURALS USA recalls
Official ID D-0620-2026 · Official record ↗
FDA Class II · Drug · June 17, 2026
Budesonide Inhalation Suspension recall — SUN PHARMACEUTICAL INDUSTRIES INC
Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0607-2026 · Official record ↗
FDA Class II · Drug · June 17, 2026
Minocycline Hydrochloride Extended-Release Tablets recall — Ascend Laboratories, LLC
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis
Company / brand: Ascend Laboratories recalls
Official ID D-0597-2026 · Official record ↗
FDA Class I · Drug · June 17, 2026
Gas-X Extra Strength recall — Haleon US Holdings LLC
Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.
Company / brand: Haleon US Holdings recalls
Official ID D-0595-2026 · Official record ↗
FDA Class II · Drug · June 17, 2026
GSMS Incorporated recall — Golden State Medical Supply Inc.
Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint.
Company / brand: Golden State Medical Supply recalls
Official ID D-0587-2026 · Official record ↗
FDA Class II · Drug · June 17, 2026
Zep recall — Zep Inc
Microbial contamination of sterile products
Company / brand: Zep recalls
Official ID D-0586-2026 · Official record ↗
FDA Class III · Drug · June 17, 2026
Primidone Tablets recall — Amneal Pharmaceuticals, LLC
Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.
Company / brand: Amneal Pharmaceuticals recalls
Official ID D-0585-2026 · Official record ↗
FDA Class II · Drug · June 17, 2026
Duloxetine Delayed-Release Capsules recall — Breckenridge Pharmaceutical, Inc.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Company / brand: Breckenridge Pharmaceutical recalls
Official ID D-0583-2026 · Official record ↗
FDA Class II · Drug · June 17, 2026
Duloxetine Delayed-Release Capsules recall — Breckenridge Pharmaceutical, Inc.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Company / brand: Breckenridge Pharmaceutical recalls
Official ID D-0582-2026 · Official record ↗
FDA Class III · Drug · June 17, 2026
Epinephrine Injection recall — Fresenius Kabi USA, LLC
Failed Impurities/Degradations Specifications
Company / brand: Fresenius Kabi USA recalls
Official ID D-0581-2026 · Official record ↗
FDA Class I · Drug · June 17, 2026
DOXOrubin Hydrochloride Liposome injection recall — SUN PHARMACEUTICAL INDUSTRIES INC
Presence of Particulate matter: Particulate matter identified as glass.
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0580-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
ANGEL branded STRAWBERRY SOFT-SERVE powder recall — SKS Copack
Products may potentially be contaminated with Salmonella.
Company / brand: SKS Copack recalls
Official ID EVT-99068-n58k06 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — Intuitive Surgical, Inc.
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching fro…
Company / brand: Intuitive Surgical recalls
Official ID Z-2310-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Sharpoint 2 recall — SSC- Surgical Specialties Corporation
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
Company / brand: SSC- Surgical Specialties recalls
Official ID Z-2309-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
TITANIUM/FLUOROPLASTIC PISTON 0 recall — Grace Medical, Inc.
Due to incorrect functional length on device labeling.
Company / brand: Grace Medical recalls
Official ID Z-2308-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Aligned Medical AMS16835 Fluids Kit RX recall — Windstone Medical Packaging, Inc.
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
Company / brand: Windstone Medical Packaging recalls
Official ID Z-2307-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
MAC 5 A4 Resting ECG Analysis System 855001-001 recall — GE Medical Systems China Co., Ltd.
Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. …
Company / brand: GE Medical Systems China Co recalls
Official ID Z-2306-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
DeRoyal Industries Inc recall — DeRoyal Industries Inc
Sterile wound dressing, lacks sterility assurance
Company / brand: DeRoyal Industries recalls
Official ID Z-2305-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis MedBank Mini REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2304-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis MedBank Tower REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2303-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis MedStation ES Tower REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2302-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis Mini Main REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2301-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis Anesthesia Station 4000 REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2300-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis Anesthesia Station ES REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2299-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis MedStation ES REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2298-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
BD Pyxis MedStation 4000 REF recall — CareFusion 303, Inc.
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Official ID Z-2297-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the M recall — Bayer Medical Care, Inc.
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock c…
Company / brand: Bayer Medical Care recalls
Official ID Z-2296-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Phothera 200 recall — Daavlin Distributing Company
Some of the Calibration/Output Certificates had the outputs reversed.
Company / brand: Daavlin Distributing Company recalls
Official ID Z-2295-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Digital Angiography System Trinias recall — Shimadzu Medical Systems
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
Company / brand: Shimadzu Medical Systems recalls
Official ID Z-2294-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Arvis Hip & Knee 2 recall — Kico Knee Innovation Company
The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Company / brand: Kico Knee Innovation Company recalls
Official ID Z-2293-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Arvis Hip & Knee 3 recall — Kico Knee Innovation Company
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Company / brand: Kico Knee Innovation Company recalls
Official ID Z-2292-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 7M20 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2291-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 7M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2290-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 7B20/15 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2289-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 7B12/12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2288-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 5M20 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2287-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 5M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2286-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 3M15 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2285-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Philips Azurion 3M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2284-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — Advanced Bionics, LLC
Due to incorrect shelf-life expiration date.
Company / brand: Advanced Bionics recalls
Official ID Z-2283-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Neptune Smart Docking Station (120V) recall — Stryker Corporation
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being ship…
Company / brand: Stryker recalls
Official ID Z-2282-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Covidien EndoStitch" Polysorb Single Use Loading Unit recall — Covidien, LP
The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.
Company / brand: Covidien recalls
Official ID Z-2281-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
CASE v7 recall — GE Medical Systems Information Technologies Inc
Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charr…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2279-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits recall — B Braun Medical Inc
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…
Company / brand: B Braun Medical recalls
Official ID Z-2278-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
Spinocan Spinal Needle procedure kits recall — B Braun Medical Inc
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…
Company / brand: B Braun Medical recalls
Official ID Z-2277-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
Spinal Needle procedure kits recall — B Braun Medical Inc
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…
Company / brand: B Braun Medical recalls
Official ID Z-2276-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
PhaseOne Antimicrobial Solution recall — Oculus Technologies of Mexico, S.A. de C.V.
The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the produc…
Company / brand: Oculus Technologies of Mexico recalls
Official ID Z-2275-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS) recall — Fresenius Kabi USA, LLC
Potential for the Cassette Loading Lever to break.
Company / brand: Fresenius Kabi USA recalls
Official ID Z-2274-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Covidien Mon-a-Therm general purpose temperature probe size recall — Covidien LLC
Temperature probe devices lack FDA clearance.
Company / brand: Covidien recalls
Official ID Z-2273-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Covidien Mon-a-Therm General Purpose Temperature Probe REF recall — Covidien LLC
Temperature probe devices lack FDA clearance.
Company / brand: Covidien recalls
Official ID Z-2272-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF recall — Covidien LLC
Temperature probe devices lack FDA clearance.
Company / brand: Covidien recalls
Official ID Z-2271-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2270-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2269-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2268-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2267-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2266-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2265-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2264-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — B Braun Medical Inc
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Official ID Z-2263-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
Brand Name recall — Baxter Healthcare Corporation
Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slow…
Company / brand: Baxter Healthcare recalls
Official ID Z-2262-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code recall — Covidien LLC
Due to customer complaint regarding incorrect display box labeling.
Company / brand: Covidien recalls
Official ID Z-2261-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2257-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2256-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2255-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2254-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2253-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2252-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2251-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2250-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2249-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3 recall — Becton Dickinson & Company
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Official ID Z-2248-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
Ivenix Infusion System (IIS) recall — Fresenius Kabi USA, LLC
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or rea…
Company / brand: Fresenius Kabi USA recalls
Official ID Z-2224-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
LVP software of the Ivenix Infusion System (IIS) recall — Fresenius Kabi USA, LLC
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless …
Company / brand: Fresenius Kabi USA recalls
Official ID Z-2223-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
Pediatric care bed recall — KAYSERBETTEN GMBH & CO. KG
If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an increased ris…
Company / brand: KAYSERBETTEN & CO. KG recalls
Official ID Z-2212-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
Atlan A350XL recall — Draeger, Inc.
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Company / brand: Draeger recalls
Official ID Z-2208-2026 · Official record ↗
FDA Class I · Medical device · June 10, 2026
Atlan A350 recall — Draeger, Inc.
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Company / brand: Draeger recalls
Official ID Z-2207-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
ARTIS Icono biplane recall — Siemens Medical Solutions USA, Inc
During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-f…
Company / brand: Siemens Medical Solutions USA recalls
Official ID Z-2206-2026 · Official record ↗
FDA Class II · Medical device · June 10, 2026
ARTIS pheno recall — Siemens Medical Solutions USA, Inc
During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-f…
Company / brand: Siemens Medical Solutions USA recalls
Official ID Z-2205-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22019700000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 1 CT UPC 22117700000 PAVILIONS CHOC recall — Albertsons Companies LLC
Contains statement does not declare Hazelnut
Company / brand: Albertsons Companies recalls
Official ID H-1074-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS COLD This is Albertson's store-m recall — Albertsons Companies LLC
Contains statement does not declare Salmon and Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1073-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21478000000 Ready Meals SALAD FRESH BERRY & SWEET CHILI Salmon SS This is Albertson's recall — Albertsons Companies LLC
Contains statement does not declare Salmon and Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1072-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 29604300000 SALMON WASABI GRILLED FS COLD This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1071-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21877300000 SALMON SWEET CHILI KOSHER PO SS COLD This is Albertson's store-made item a recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1070-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21919300000 SALMON LEMON PEPPER KOSHER PO SS COLD This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1069-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23180600000 SALMON KABOB With CITRUS LEMON MARINADE This is Albertson's store-made ite recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1068-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23151700000 SALMON FILLET With CITRUS LEMON MARINADE This is Albertson's store-made it recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1067-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23090400000 SALMON FILLET POLLO ASADO MARINADE This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1066-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23077600000 SALMON FILLET CARNE ASADA MARINADE This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1065-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23041600000 SALMON COHO FILLET GARLIC HERB SEASONED This is Albertson's store-made ite recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1064-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23100200000 SALMON ATLANTIC PORTION PIRI PIRI MARINADE This is Albertson's store-made recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1063-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23098000000 SALMON ATLANTIC PORTION CA ORANGE MARINADE This is Albertson's store-made recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1062-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21497700000 Ready Meals SALMON POT ROSETTES & ROSEMARY SS COLD This is Albertson's sto recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1061-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21382900000 Ready Meals SALMON PESTO With ASPARAGUS SS COLD This is Albertson's store- recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1060-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 29120700000 Ready Meals SALAD SMOKED SALMON & FETA PASTA SS UPC 29137800000 SALAD SMOK recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1059-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21494500000 Ready Meals MEAL SALMON With LEMON CAPELLINI PASTA SS This is Albertson's recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1058-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21136500000 Ready Meals BOWL SALMON TERIYAKI SS COLD UPC 21477800000 Ready Meals BOWL recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1057-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21292200000 SALMON CAJUN PREMIUM FS COLD This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1056-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21495100000 Ready Meals MEAL SALMON CAJUN SS COLD This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1055-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21142400000 MEAL CAJUN SALMON & SPANISH RICE SS COLD This is Albertson's store-made it recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1054-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23258300000 BURGER WILD SALMON FETA SPINACH This is Albertson's store-made item and so recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1053-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 29251100000 Ready Meals TUNA SALAD & PEPPER JACK CHEESE SNACKER This is Albertson's st recall — Albertsons Companies LLC
Contains statement does not declare Tuna
Company / brand: Albertsons Companies recalls
Official ID H-1052-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21843300000 READY MEALS TUNA SALAD & MUENSTER CHEESE SNACK PACK This is Albertson's st recall — Albertsons Companies LLC
Contains statement does not declare Tuna
Company / brand: Albertsons Companies recalls
Official ID H-1051-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21500300000 READY MEALS QUAD TUNA SALAD This is Albertson's store-made item and sold b recall — Albertsons Companies LLC
Contains statement does not declare Tuna
Company / brand: Albertsons Companies recalls
Official ID H-1050-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 29132100000 KITCHEN SNACKER SALAD TUNA PICKLE This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Tuna
Company / brand: Albertsons Companies recalls
Official ID H-1049-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 25748400000 STICKY BUNS GOURMET WALNUT 4CT This is Albertson's store-made item and sol recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1048-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 23952700000 POKE AHI LIMU UPC 23506700000 POKE AHI LIMU PREVIOUSLY FROZEN - CO UPC 239 recall — Albertsons Companies LLC
Contains statement does not declare Tuna
Company / brand: Albertsons Companies recalls
Official ID H-1047-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21600500000 READY MEALS SALAD PREMIUM BROCCOLI SS This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Cashew
Company / brand: Albertsons Companies recalls
Official ID H-1046-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21425300000 READY MEALS SALAD KALE MANGO & COCONUT SS UPC 21042400000 SALAD KALE MANGO recall — Albertsons Companies LLC
Contains statement does not declare Cashew
Company / brand: Albertsons Companies recalls
Official ID H-1045-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21409600000 READY MEALS MEATLOAF SS COLD This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1044-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 29502200000 Ready Meals BOWL GRAIN SALMON QUINOA LENTIL SS COLD This is Albertson's st recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1043-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21330300000 Ready Meals BAKED POLLOCK 4CT SS COLD This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Pollock
Company / brand: Albertsons Companies recalls
Official ID H-1042-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 25800800000 POP DOTS COCO & HAZELNUT 6CT This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare hazelnut
Company / brand: Albertsons Companies recalls
Official ID H-1041-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23308200000 TILAPIA TORTILLA CRUSTED This is Albertson's store-made item and sold by r recall — Albertsons Companies LLC
Contains statement does not declare Tilapia
Company / brand: Albertsons Companies recalls
Official ID H-1040-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21234900000 TILAPIA PARMESAN CRUSTED SS COLD This is Albertson's store-made item and s recall — Albertsons Companies LLC
Contains statement does not declare Tilapia
Company / brand: Albertsons Companies recalls
Official ID H-1039-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29472300000 SALAD KALE BERRY FETA FS COLD UPC 29472100000 Ready Meals SALAD KALE BERRY recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1038-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29361000000 KITCHEN SALAD TURKEY POPPYSEED SS COLD UPC 29360900000 KITCHEN SALAD TURKE recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1037-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21870200000 KITCHEN SALAD SESAME ASIAN LARGE SS COLD UPC 27817500000 Ready Meals SALAD recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1036-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29787500000 KITCHEN SALAD SPRING LARGE This is Albertson's store-made item and sold by recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1035-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 24144500000 Ready Meals PEANUT BUTTER CHOCOLATE CHIP BAR With PRETZEL This is Albertso recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1034-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25688000000 PIE PEACH MELBA 9IN This is Albertson's store-made item and sold by unit a recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1033-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21176300000 MEAT PIE PORK 4CT SS COLD UPC 21025900000 PIE PORK FS COLD This is Alberts recall — Albertsons Companies LLC
Contains statement does not declare Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1032-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21299900000 LOX AVOCADO TOAST FS COLD This is Albertson's store-made item and sold by recall — Albertsons Companies LLC
Contains statement does not declare Salmon
Company / brand: Albertsons Companies recalls
Official ID H-1031-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22304700000 PLATTER SNACK CHEWIE SUSANS THUMBPRINTS This is Albertson's store-made ite recall — Albertsons Companies LLC
Contains statement does not declare Pecan
Company / brand: Albertsons Companies recalls
Official ID H-1030-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22650200000 PLATTER LOAF SLC 20CT This is Albertson's store-made item and sold by unit recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1029-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25511500000 PLATTER BROWNIES ASSORTED SEASONAL This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1028-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25081900000 PLATTER PASTRY MINI BREAKFAST 28CT This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1027-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 27837800000 PLATTER CHEESES OF FRANCE This is Albertson's store-made item and sold by recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1026-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21380100000 Ready Meals WOK PAD THAI CHICKEN WITH POT STICKERS SS This is Albertson's recall — Albertsons Companies LLC
Contains statement does not declare Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1025-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21379600000 Ready Meals WOK PAD THAI CHICKEN WITH EGG ROLL SS COLD This is Albertson's recall — Albertsons Companies LLC
Contains statement does not declare Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1024-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21208300000 Ready Meals WOK PAD THAI CHICKEN SS COLD This is Albertson's store-made it recall — Albertsons Companies LLC
Contains statement does not declare Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1023-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21195200000 READY MEALS SALAD FRESH BERRY & CHICKEN SS COLD This is Albertson's store- recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1022-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 27163100000 Kitchen SALAD GRILLED CHICKEN SS COLD This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1021-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29433900000 Kitchen SALAD CHICKEN STRIP This is Albertson's store-made item and sold b recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-1020-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 24512800000 SALAD CHICKEN CAESAR UPC 29854600000 Kitchen SALAD CHICKEN CAESAR This is recall — Albertsons Companies LLC
Contains statement does not declare Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1019-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29787600000 Kitchen SALAD CAESAR LARGE SS COLD UPC 21543200000 Kitchen SALAD CAESAR SM recall — Albertsons Companies LLC
Contains statement does not declare Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1018-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21633500000 READY MEALS SALAD APPLE WALDORF SS UPC 29824500000 Kitchen SALAD APPLE WAL recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1017-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21163600000 Ready Meals SALAD WALDORF SS This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-1016-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Crab and Pollock
Company / brand: Albertsons Companies recalls
Official ID H-1015-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29477800000 Ready Meals SALAD SEAFOOD CAJUN SS COLD UPC 29477600000 SALAD SEAFOOD CAJU recall — Albertsons Companies LLC
Contains statement does not declare Crab and Pollock
Company / brand: Albertsons Companies recalls
Official ID H-1014-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 23625000000 FISH HOUSE PREMIUM SEAFOOD SALAD UPC 21431200000 Ready Meals SALAD SEAFOOD recall — Albertsons Companies LLC
Contains statement does not declare Crab
Company / brand: Albertsons Companies recalls
Official ID H-1013-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 27183100000 Ready Meals DUO SEAFOOD SALAD W/CRACKERS This is Albertson's store-made it recall — Albertsons Companies LLC
Contains statement does not declare Whiting
Company / brand: Albertsons Companies recalls
Official ID H-1012-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21535300000 TEMPURA SHRIMP THAI SWEET CHILI SAUCE SS This is Albertson's store-made it recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1011-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23070400000 SHRIMP SKEWER MEDIUM RAW CILANTRO LIME This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1010-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23036500000 SHRIMP P&D OLD BAY SEASONED This is Albertson's store-made item and sold b recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1009-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23044100000 SHRIMP P&D CAJUN SEASONED This is Albertson's store-made item and sold by recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1008-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23025600000 SHRIMP MEDIUM SWEET CHILI MARINADE This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1007-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23180100000 SHRIMP KABOB 16-20 CT W/KUNG PAO MRND This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1006-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23179700000 SHRIMP KABOB 16-20 CT With JAMAICAN JRK MARINADE This is Albertson's store recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1005-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23152800000 SHRIMP 41-50 P&D With JAMAICAN JERK MARINADE 5% This is Albertson's store- recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1004-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23150400000 SHRIMP 41-50 P&D With CITRUS LEMON MARINADE 5% This is Albertson's store-m recall — Albertsons Companies LLC
Contains statement does not declare Shrimp.
Company / brand: Albertsons Companies recalls
Official ID H-1003-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 23168600000 SHRIMP 41-50 P&D With CILANTRO LIME MARINADE 5% This is Albertson's store- recall — Albertsons Companies LLC
Contains statement does not declare Shrimp and Anchovy
Company / brand: Albertsons Companies recalls
Official ID H-1002-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 23043800000 SHRIMP 16-20 KABOB POLLO ASADA MARINADE This is Albertson's store-made ite recall — Albertsons Companies LLC
Contains statement does not declare Shrimp
Company / brand: Albertsons Companies recalls
Official ID H-1001-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 23245700000 SHRIMP & SURIMI CEVICHE FRESH This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Sea Bream
Company / brand: Albertsons Companies recalls
Official ID H-1000-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 29473400000 SALAD LEMON CAPELLINI With GRILLED SHRIMP FS This is Albertson's store-mad recall — Albertsons Companies LLC
Contains statement does not declare Shrimp
Company / brand: Albertsons Companies recalls
Official ID H-0999-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21963800000 Ready Meals CHIMICHURRI SHRIMP BOWL SS COLD This is Albertson's store-made recall — Albertsons Companies LLC
Contains statement does not declare Shrimp
Company / brand: Albertsons Companies recalls
Official ID H-0998-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21467900000 Ready Meals BOWL SOUTHWEST SHRIMP LARGE SS COLD UPC 21963600000 Ready Meal recall — Albertsons Companies LLC
Contains statement does not declare Shrimp
Company / brand: Albertsons Companies recalls
Official ID H-0997-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 23285600000 IMITATION CRAB AND SHRIMP SALAD SRIRACHA This is Albertson's store-made it recall — Albertsons Companies LLC
Contains statement does not declare Pollock
Company / brand: Albertsons Companies recalls
Official ID H-0996-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 23285300000 IMITATION CRAB AND SHRIMP SALAD This is Albertson's store-made item and so recall — Albertsons Companies LLC
Contains statement does not declare Pollock
Company / brand: Albertsons Companies recalls
Official ID H-0995-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29344500000 TWISTED BLISS PRETZEL TRAY This is Albertson's store-made item and sold by recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0994-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29133000000 TRAY COCKTAIL This is Albertson's store-made item and sold by unit at poin recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0993-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29138800000 TRAY CHARCUTERIE ELEGANT This is Albertson's store-made item and sold by u recall — Albertsons Companies LLC
Contains statement does not declare Pistachio
Company / brand: Albertsons Companies recalls
Official ID H-0992-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0991-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 27841000000 Ready Meals TRAY BRIE & BLEU CHEESE LARGE This is Albertson's store-made i recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0990-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 27852000000 Ready Meals BRIE ALMOND TRAY SMALL COLD This is Albertson's store-made ite recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0989-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29168800000 CARVING TRAY 16IN FS This is Albertson's store-made item and sold by unit recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-0988-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25047100000 ANDRONICO'S SWEET START CATERING TRAY LARGE This is Albertson's store-made recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-0987-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25606600000 PARFAIT CUP DUBAI CHOCOLATE This is Albertson's store-made item and sold b recall — Albertsons Companies LLC
Contains statement does not declare Pistachio
Company / brand: Albertsons Companies recalls
Official ID H-0986-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22321200000 MUFFINS PISTACHIO 2CT UPC 22770600000 MUFFINS PISTACHIO 4CT This is Albert recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-0985-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 22761900000 MUFFINS ALMOND POPPYSEED 4CT This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0984-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25524000000 MUFFINS STICKY BRAN 4CT This is Albertson's store-made item and sold by un recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-0983-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE This is Albertson's store-made i recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-0982-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT This is Albertson's store-made recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-0981-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22454900000 MUFFINS BANANA NUT 2CT UPC 22120200000 MUFFINS BANANA NUT 4CT This is Albe recall — Albertsons Companies LLC
Contains statement does not declare Walnut
Company / brand: Albertsons Companies recalls
Official ID H-0980-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 29219100000 Ready Meals SANDWICH HAGGIE STORE CLASSIC TUNA SS COLD This is Albertson's recall — Albertsons Companies LLC
Contains statement does not declare Tuna
Company / brand: Albertsons Companies recalls
Official ID H-0979-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 29259700000 KITCHEN TRAY SUB SANDWICH SS This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Pistachio
Company / brand: Albertsons Companies recalls
Official ID H-0978-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 21243500000 KITCHEN SANDWICH ITALIAN SUPER SUB SS COLD This is Albertson's store-made recall — Albertsons Companies LLC
Contains statement does not declare Pistachio
Company / brand: Albertsons Companies recalls
Official ID H-0977-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21788400000 Ready Meals SANDWICH TUNA SALAD CROISSANT SS COLD This is Albertson's stor recall — Albertsons Companies LLC
Contains statement does not declare TUNA
Company / brand: Albertsons Companies recalls
Official ID H-0976-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 21914600000 KITCHEN SANDWICH CROISSANT CHICKEN CASHEW SS This is Albertson's store-mad recall — Albertsons Companies LLC
Contains statement does not declare Cashew
Company / brand: Albertsons Companies recalls
Official ID H-0975-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25678000000 CROISSANTS DUBAI CHOCOLATE 2CT This is Albertson's store-made item and sol recall — Albertsons Companies LLC
Contains statement does not declare Pistachio
Company / brand: Albertsons Companies recalls
Official ID H-0974-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 25317100000 CROISSANTS ALMOND RASPBERRY FILLED 4CT This is Albertson's store-made item recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0973-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 28586600000 CROISSANT ALMOND UPC 22102100000 CROISSANTS ALMOND 4 CT UPC 29671400000 HG recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0972-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 26911700000 COOKIES OATMEAL RAISIN 10CT This is Albertson's store-made item and sold b recall — Albertsons Companies LLC
Contains statement does not declare Almond
Company / brand: Albertsons Companies recalls
Official ID H-0971-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22358600000 COOKIES MEXICAN WEDDING 8 CT This is Albertson's store-made item and sold recall — Albertsons Companies LLC
Contains statement does not declare Pecan
Company / brand: Albertsons Companies recalls
Official ID H-0970-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22730900000 COOKIES COWBOY 18CT This is Albertson's store-made item and sold by unit a recall — Albertsons Companies LLC
Contains statement does not declare Pecan
Company / brand: Albertsons Companies recalls
Official ID H-0969-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25185700000 COOKIE GOURMET DUBAI 1CT This is Albertson's store-made item and sold by u recall — Albertsons Companies LLC
Contains statement does not declare Pistachio.
Company / brand: Albertsons Companies recalls
Official ID H-0968-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25814700000 CAKE BOSTON CREME DUBAI 5IN This is Albertson's store-made item and sold b recall — Albertsons Companies LLC
Contains statement does not declare Pistachio.
Company / brand: Albertsons Companies recalls
Official ID H-0967-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 22749800000 CAKE BOSTON ALMOND This is Albertson's store-made item and sold by unit at recall — Albertsons Companies LLC
Contains statement does not declare Almond.
Company / brand: Albertsons Companies recalls
Official ID H-0966-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 25394400000 CAKE PISTACHIO SHAPED DESSERT 1CT This is Albertson's store-made item and recall — Albertsons Companies LLC
Contains statement does not declare Pistachio.
Company / brand: Albertsons Companies recalls
Official ID H-0965-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 22394700000 Cake Almond Raspberry Pavillions 2-layer This is Albertson's store-made it recall — Albertsons Companies LLC
Contains statement does not declare Almond.
Company / brand: Albertsons Companies recalls
Official ID H-0964-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer recall — Albertsons Companies LLC
Contains statement does not declare Almond.
Company / brand: Albertsons Companies recalls
Official ID H-0963-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25491700000 Cake Pav Chocolate Lady Madeleines Strawberry recall — Albertsons Companies LLC
Contains statement does not declare Almond.
Company / brand: Albertsons Companies recalls
Official ID H-0962-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle recall — Albertsons Companies LLC
Contains statement does not declare Hazelnut.
Company / brand: Albertsons Companies recalls
Official ID H-0961-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22253500000 Cake Bar Artisan White Strawberry Small recall — Albertsons Companies LLC
Contains statement does not declare Almond.
Company / brand: Albertsons Companies recalls
Official ID H-0960-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22418000000 Platter Catering Loaf Cake Slice recall — Albertsons Companies LLC
Contains statement does not declare Walnut.
Company / brand: Albertsons Companies recalls
Official ID H-0959-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 25216200000 Cheesecake Slice Colossal Dubai recall — Albertsons Companies LLC
Contains statement does not declare pistachio.
Company / brand: Albertsons Companies recalls
Official ID H-0958-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 28848900000 Cake Yellow Fudge Pecan 1/2 8IN This is Albertson's store-made item and so recall — Albertsons Companies LLC
Contains statement does not declare pecan.
Company / brand: Albertsons Companies recalls
Official ID H-0957-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
UPC 28832500000 Cake Yellow Caramel Pecan 1/2 8IN UPC 28831600000 Cake Yellow Caramel Peca recall — Albertsons Companies LLC
Contains statement does not declare pecan.
Company / brand: Albertsons Companies recalls
Official ID H-0956-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22679400000 CAKE CRAVIN CARROT 8IN 1-layer This is Albertson's store-made item and is recall — Albertsons Companies LLC
Contains statement does not declare pecan.
Company / brand: Albertsons Companies recalls
Official ID H-0955-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
UPC 22655200000 CAKE CARROT 8IN 2-Layer UPC 27813200000 CAKE CARROT 8IN 2-Layer These are recall — Albertsons Companies LLC
Contains statement does not declare pecan or walnut.
Company / brand: Albertsons Companies recalls
Official ID H-0954-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
001165 recall — University of California Health Milk Bank
Product is potentially contaminated with foreign material (plastic particles).
Company / brand: University of California Health Milk Bank recalls
Official ID H-0948-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
Lunds & Byerly's Curry Powder Sweet recall — J and J Bunting, Inc
Sesame Seeds White were labeled as Curry Powder Sweet.
Company / brand: J and J Bunting recalls
Official ID H-0914-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Cold Prep Cream Sauce recall — The Coffee Connexion Co., Inc
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
Company / brand: The Coffee Connexion Co recalls
Official ID H-0910-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Alfredo Sauce recall — The Coffee Connexion Co., Inc
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
Company / brand: The Coffee Connexion Co recalls
Official ID H-0909-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Aramark Cheese Sauce New & Improved recall — The Coffee Connexion Co., Inc
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
Company / brand: The Coffee Connexion Co recalls
Official ID H-0908-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
1) Cheese Sauce Mix recall — The Coffee Connexion Co., Inc
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
Company / brand: The Coffee Connexion Co recalls
Official ID H-0907-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Raw Shelled Peanuts (Runner Type) 2 recall — Wilco Peanut Co
Undeclared Tree Nut Allergen
Company / brand: Wilco Peanut Co recalls
Official ID H-0906-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
SECOND NATURE KETO CRUNCH SMART MIX recall — SECOND NATURE BRAND
The product may contain undeclared allergens (cashews, pistachios), and dried cherries.
Company / brand: SECOND NATURE BRAND recalls
Official ID H-0905-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
Market of Choice Vegan Kale Caesar Salad recall — Market of Choice Inc
Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame.
Company / brand: Market of Choice recalls
Official ID H-0904-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag recall — Hometown Food Company
Undeclared egg
Company / brand: Hometown Food Company recalls
Official ID H-0903-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
My Wife's Slaw Jalapeno Heat recall — Jesse Withrow
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
Company / brand: Jesse Withrow recalls
Official ID H-0902-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
My Wife's Slaw recall — Jesse Withrow
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
Company / brand: Jesse Withrow recalls
Official ID H-0901-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
Betaine Anhydrous recall — Creative Compounds, LLC
Possible carbon steel foreign material (1-2mm)
Company / brand: Creative Compounds recalls
Official ID H-0900-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Hellas Meze Golden Smoked Whole Herring recall — Terra Medi LLC
Un-eviscerated fish may be contaminated with clostridium botulinum
Company / brand: Terra Medi recalls
Official ID H-0899-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Enoki Mushroom recall — IQ PRODUCE, LLC
Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
Company / brand: IQ PRODUCE recalls
Official ID H-0898-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
STRAUS FAMILY CREAMERY Mint Chip ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced recall — Straus Family Creamery
Potential contamination with foreign objects (metal pieces).
Company / brand: Straus Family Creamery recalls
Official ID H-0897-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
STRAUS FAMILY CREAMERY Dutch Chocolate ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) P recall — Straus Family Creamery
Potential contamination with foreign objects (metal pieces).
Company / brand: Straus Family Creamery recalls
Official ID H-0896-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
STRAUS FAMILY CREAMERY Cookie Dough ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produ recall — Straus Family Creamery
Potential contamination with foreign objects (metal pieces).
Company / brand: Straus Family Creamery recalls
Official ID H-0895-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
STRAUS FAMILY CREAMERY Strawberry ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) ONE PI recall — Straus Family Creamery
Potential contamination with foreign objects (metal pieces).
Company / brand: Straus Family Creamery recalls
Official ID H-0894-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produ recall — Straus Family Creamery
Potential contamination with foreign objects (metal pieces).
Company / brand: Straus Family Creamery recalls
Official ID H-0893-2026 · Official record ↗
FDA Class III · Food · June 10, 2026
Yunker(branded) Energy & Health Herbal Supplement with Vitamins recall — Sato Pharmaceutical Inc.
Product does not meet label claim for Vitamin E.
Company / brand: Sato Pharmaceutical recalls
Official ID H-0892-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
a2 Platinum Premium infant formula Milk-based Powder with Iron 31 recall — The a2 Milk Company
Possible contamination with Cereulide toxin.
Company / brand: The a2 Milk Company recalls
Official ID H-0891-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
White Cheddar Seasoning packaged in the following sized containers recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0890-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
#0083004 Ranch Seasoning recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0889-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
#003740 Dill & Garlic Seasoning recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0888-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
#003020 Sour Cream & Onion recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0887-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Popping Topping recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0886-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
#800414/003729Butter Parsley recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0885-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Karlsburger Kitchens Garlic N Cheese Topper recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0884-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
#007415 Fiery Hot recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0883-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
#009530 Ranch Seasoning recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0882-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
#007560 Fiery Hot Seasoning (Reduced Salt) recall — JCB Flavors, LLC
Products may be potentially contaminated with Salmonella.
Company / brand: JCB Flavors recalls
Official ID H-0881-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
72% CACAO CHOCOLATE WITH DATE SUGAR WAFERS Ingredients recall — Guittard Chocolate Company
Potential contamination with Salmonella
Company / brand: Guittard Chocolate Company recalls
Official ID H-0861-2026 · Official record ↗
FDA Class I · Food · June 10, 2026
Malazi 100% PURE SUDANESE SESAME Tahina G recall — Nassar Investment Company LLC
Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.
Company / brand: Nassar Investment Company recalls
Official ID H-0860-2026 · Official record ↗
FDA Class II · Food · June 10, 2026
cafe nouria blueberry muffin NET WT recall — The Brownie Baker Inc.
Undeclared walnuts
Company / brand: The Brownie Baker recalls
Official ID H-0859-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Xyvona (levorphanol tartrate tablets) recall — SUN PHARMACEUTICAL INDUSTRIES INC
Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0599-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Xyvona (levorphanol tartrate tablets) recall — SUN PHARMACEUTICAL INDUSTRIES INC
Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0598-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
Niacin Extended-release Tablets recall — Lannett Company Inc.
Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.
Company / brand: Lannett Company recalls
Official ID D-0584-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
TopCare health recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0579-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
TopCare health recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0578-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
EQUALINE ultra strength recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0577-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
EQUALINE extra strength recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0576-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
GOODSENSE Ultra Strength recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0575-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
GOODSENSE Extra Strength recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0574-2026 · Official record ↗
FDA Class II · Drug · June 10, 2026
H recall — Guardian Drug Co. Inc.
Presence of foreign substance: small metallic particles in chewable tablets.
Company / brand: Guardian Drug Co recalls
Official ID D-0573-2026 · Official record ↗
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
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FDA last checked October 22, 2026 at 12:00 PM UTC.