Fresh Recalls

Latest recalls — page 9

Browse the most recent U.S. safety recalls in our connected official government data.

3,525 recalls in our current data. Showing 801–900, newest first.

FDA Class II · Drug · September 9, 2026

THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall — Allies Group Inc.

Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.

Company / brand: Allies Group recalls

Official ID D-0824-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall — Allies Group Inc.

Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.

Company / brand: Allies Group recalls

Official ID D-0823-2026 · Official record ↗

FDA Class III · Drug · September 9, 2026

Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg recall — Bionpharma Inc.

Presence of Foreign Tablets/Capsules

Company / brand: Bionpharma recalls

Official ID D-0822-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Daptomycin recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0821-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Vancomycin Injection recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0820-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Vasopressin recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0819-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Clindamycin Injection USP in 5% Dextrose recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0818-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Clindamycin Injection USP in 5% Dextrose recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0817-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Clindamycin Phosphate in 0 recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0816-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Clindamycin Injection USP in 5% Dextrose recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0815-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Nexterone (amiodarone HCI) recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0814-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

CARDENE IV (Nicardipine Hydrochloride) in 0 recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0813-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Pantoprazole Sodium in 0 recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0812-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Vasopressin recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0811-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Dexmedetomidine Hydrochloride in 0 recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0810-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Famotidine Injection in Sodium Chloride Injection recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0809-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Clindamycin Injection USP in 5% Dextrose recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0808-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Daptomycin recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0807-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

MYXREDLIN recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0806-2026 · Official record ↗

FDA Class II · Drug · September 9, 2026

Vancomycin Injection recall — Baxter Healthcare Corporation

CGMP Deviations

Company / brand: Baxter Healthcare recalls

Official ID D-0805-2026 · Official record ↗

NHTSA · Vehicle · September 7, 2026

Bombardier Recreational Products Electrical System recall (26V575000)

An inoperative instrument cluster will fail to display critical safety information, such as vehicle speed and warning lights, increasing the risk of a crash.

Company / brand: Bombardier Recreational Products recalls

Official ID 26V575000 · Official record ↗

NHTSA · Vehicle · September 5, 2026

Renegade Classic recall (26V574000)

An overheated printed circuit board increases the risk of a fire.

Company / brand: Kibbi recalls

Official ID 26V574000 · Official record ↗

NHTSA · Vehicle · September 3, 2026

Nova Bus Engine And Engine Cooling recall (26V573000)

An unexpected engine shut down can increase the risk of a crash. Additionally, transferring passengers from the disabled bus can increase the risk of injury.

Company / brand: Nova Bus recalls

Official ID 26V573000 · Official record ↗

NHTSA · Vehicle equipment · September 3, 2026

Casco Coolant Level(Ecl) Sensor recall (26E062000)

An unexpected engine shut down can increase the risk of a crash. Additionally, transferring passengers from the disabled bus can increase the risk of injury.

Company / brand: Nova Bus recalls

Official ID 26E062000 · Official record ↗

CPSC · Bicycles & Accessories · September 3, 2026

MONDRAKER USA Recalls Mountain Bicycles Equipped with ONOFF S9 Carbon MTB Handlebars Due to Risk of Serious Injury or Death from Fall Hazard

The affected handlebars may crack or fracture during use, which can lead to loss of control, posing a risk of serious injury or death from fall hazard.

Company / brand: MONDRAKER USA recalls

Official ID 26746 · Official notice ↗

CPSC · Cleaners/Cleaning Products · September 3, 2026

Clorox Puerto Rico Recalls 6 Million Scented Mistolin and Lestoil Multi-Purpose Cleaners Due to Risk of Exposure to Bacteria

The recalled products may contain bacteria, including Pseudomonas aeruginosa, which is an environmental organism found widely in soil and water. People with weakened immune systems…

Company / brand: Clorox Manufacturing Company of Puerto Rico recalls

Official ID 26741 · Official notice ↗

CPSC · Adapter/Power Supply/Charger/Battery · September 3, 2026

Truststone Group Recalls XO Poppy Power Trip Magnetic Wireless Power Banks Due to Fire and Burn Hazards; Sold Exclusively at TJX and Marshalls Stores

The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.

Company / brand: Truststone Group of New York recalls

Official ID 26740 · Official notice ↗

CPSC · Toys · September 3, 2026

Skip Hop Recalls Baby Sesame Street Elmo Silicone Teethers Due to Risk of Serious Injury or Death from Choking Hazard

The black eyes can detach from the recalled teether if frozen, posing a risk of serious injury or death from a choking hazard.

Company / brand: The William Carter Company recalls

Official ID 26739 · Official notice ↗

CPSC · Squeeze Or Squeaker Toys · September 3, 2026

GIHNJSI Squeezy Dumplings Toys Recalled Due to Serious Ingestion, Choking and Obstruction Hazards; Sold on Amazon by Chenyuanhui

The squeezy toys contain water beads. If ingested, water beads expand and can pose deadly ingestion, choking, and intestinal obstruction hazards inside a child’s body, resulting in…

Company / brand: Xiamen Liuhui Electric Technology Co recalls

Official ID 26738 · Official notice ↗

CPSC · Squeeze Or Squeaker Toys · September 3, 2026

OKK Trading Recalls Rainbow Mystery Squishy Bun Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys

The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly ingestion hazard. If …

Company / brand: OKK Trading recalls

Official ID 26737 · Official notice ↗

CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · September 3, 2026

Gizoon Direct Recalls Six-Drawer Double Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…

Company / brand: Airiva recalls

Official ID 26736 · Official notice ↗

CPSC · Chairs, Not Specified · September 3, 2026

Branch Recalls Ergonomic Chairs Due to Fall Hazard

The backrests of the chairs can detach, posing a fall hazard to consumers.

Company / brand: Bureau Office recalls

Official ID 26735 · Official notice ↗

CPSC · Air Conditioners · September 3, 2026

Daikin Comfort Technologies Manufacturing Recalls Amana Through-The-Wall Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire

The snubber circuit can emit flames if it shorts, posing a risk of serious injury due to fire hazard.

Company / brand: Daikin Comfort Technologies Manufacturing recalls

Official ID 26734 · Official notice ↗

CPSC · Adult Bed Rails · September 3, 2026

Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Loyoda Direct and Loyoda

The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of th…

Company / brand: Fangzhou Overseas Consulting Shenzhen Co recalls

Official ID 26733 · Official notice ↗

CPSC · Toys & Children · September 3, 2026

SHEIN Distribution Corporation Recalls Spiral Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Ball Ban

The toys violate the small ball ban because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.

Company / brand: SHEIN Distribution of Los Angeles recalls

Official ID 26732 · Official notice ↗

CPSC · Speakers · September 3, 2026

Audio Partnership Recalls Cambridge Audio Yoyo (M) Portable Bluetooth Speakers Due to Fire Hazard

The lithium-ion batteries in the Cambridge Audio Yoyo (M) Portable Bluetooth Speaker can overheat, posing a fire hazard.

Company / brand: Audio Partnership recalls

Official ID 26731 · Official notice ↗

CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · September 3, 2026

Nanjing Wu Hai Smart Home Appliance Store Recalls Alanca 6-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…

Company / brand: Nanjing Wu Hai Smart Home Appliance Store recalls

Official ID 26730 · Official notice ↗

NHTSA · Vehicle · September 2, 2026

Toyota Motor Engineering & Manufacturing Equipment recall (26V571000)

A vehicle with an incorrect maximum capacity weight value may be overloaded, increasing the risk of a crash.

Company / brand: Toyota Motor Engineering & Manufacturing recalls

Official ID 26V571000 · Official record ↗

NHTSA · Vehicle · September 2, 2026

Toyota C-HR recall (26V570000)

An unexpected loss of drive power increases the risk of a crash.

Company / brand: Toyota Motor Engineering & Manufacturing recalls

Official ID 26V570000 · Official record ↗

FDA Not Yet Classified · Drug · September 2, 2026

Ibuprofen recall — Safecor Health, LLC

Cross Contamination with Other Products

Company / brand: Safecor Health recalls

Official ID EVT-99666-wagogx · Official record ↗

FDA Not Yet Classified · Food · September 2, 2026

Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICA recall — Africando Foods LLC

Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list

Company / brand: Africando Foods recalls

Official ID EVT-99642-1ffccqp · Official record ↗

FDA Class II · Medical device · September 2, 2026

FRU (Field replaceable unit) recall — GE Medical Systems Information Technologies Inc

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…

Company / brand: GE Medical Systems Information Technologies recalls

Official ID Z-3039-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

PORTRAIT CORE SERVICES SOFTWARE V1 recall — GE Medical Systems Information Technologies Inc

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…

Company / brand: GE Medical Systems Information Technologies recalls

Official ID Z-3038-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

PORTRAIT COMPUTE AND CORE SERVICES V1 recall — GE Medical Systems Information Technologies Inc

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…

Company / brand: GE Medical Systems Information Technologies recalls

Official ID Z-3037-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

PORTRAIT CORE SERVICES SOFTWARE V1 recall — GE Medical Systems Information Technologies Inc

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…

Company / brand: GE Medical Systems Information Technologies recalls

Official ID Z-3036-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

POWERSEAL 5 MM (in diameter) 23 CM (long) recall — Olympus Corporation of the Americas

Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.

Company / brand: Olympus of the Americas recalls

Official ID Z-3035-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

ORT300 recall — IMRIS Imaging Inc

The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This…

Company / brand: IMRIS Imaging recalls

Official ID Z-3034-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

ORT200 recall — IMRIS Imaging Inc

The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This…

Company / brand: IMRIS Imaging recalls

Official ID Z-3033-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

healthmark ProChek-W Protein Test for Robotic Arms recall — Healthmark Industries Co., Inc.

Test manufactured with an expired ingredient which may present as either a false negative or positive.

Company / brand: Healthmark Industries Co recalls

Official ID Z-3032-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

healthmark ProChek-II recall — Healthmark Industries Co., Inc.

Test manufactured with an expired ingredient which may present as either a false negative or positive.

Company / brand: Healthmark Industries Co recalls

Official ID Z-3031-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

FUJIFILM Synapse PACS software v7 recall — FUJIFILM Healthcare Americas Corporation

Software issue may cause the ruler measurement to be inaccurate.

Company / brand: FUJIFILM Healthcare Americas recalls

Official ID Z-3030-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3029-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3028-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3027-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3026-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3025-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3024-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3023-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3022-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3021-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3020-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline convenience kits labeled as recall — Medline Industries, LP

Kits contain a potentially contaminated component which were recalled by the manufacturer

Company / brand: Medline Industries recalls

Official ID Z-3019-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5 recall — ConMed Corporation

Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.

Company / brand: ConMed recalls

Official ID Z-3018-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Fresenius Medical Care recall — Fresenius Medical Care Renal Therapies Group, LLC

Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis m…

Company / brand: Fresenius Medical Care Renal Therapies Group recalls

Official ID Z-3017-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Grandio Universal Nano-Hybrid Restorative Material - Capsules 0 recall — Henry Schein Inc.

Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

Company / brand: Henry Schein recalls

Official ID Z-3016-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Structur 2 SC Temporary Resin Cartridge Refill 75Gm recall — Henry Schein Inc.

Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

Company / brand: Henry Schein recalls

Official ID Z-3015-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluo recall — Canon Medical System, USA, INC.

Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.

Company / brand: Canon Medical System recalls

Official ID Z-3014-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Midmark Digital ECG HD+12 recall — Midmark Corporation

A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.

Company / brand: Midmark recalls

Official ID Z-3013-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Midmark IQecg Digital ECG recall — Midmark Corporation

A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.

Company / brand: Midmark recalls

Official ID Z-3012-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Company / brand: AVID Medical recalls

Official ID Z-3011-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Company / brand: AVID Medical recalls

Official ID Z-3010-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Company / brand: AVID Medical recalls

Official ID Z-3009-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Company / brand: AVID Medical recalls

Official ID Z-3008-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Company / brand: AVID Medical recalls

Official ID Z-3007-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Company / brand: AVID Medical recalls

Official ID Z-3006-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Brand Name recall — AVID Medical, Inc.

Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.

Company / brand: AVID Medical recalls

Official ID Z-3005-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Merge PACS and Merge OrthoPACS recall — Merge Healthcare, Inc.

Software issue may cause measurements to be displayed inaccurately.

Company / brand: Merge Healthcare recalls

Official ID Z-3004-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

American Contract System Convenience Kit recall — American Contract Systems Inc

The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…

Company / brand: American Contract Systems recalls

Official ID Z-3003-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

American Contract System Convenience Kits recall — American Contract Systems Inc

The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…

Company / brand: American Contract Systems recalls

Official ID Z-3002-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

American Contract System Convenience Kit recall — American Contract Systems Inc

The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…

Company / brand: American Contract Systems recalls

Official ID Z-3001-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

American Contract System Convenience Kit recall — American Contract Systems Inc

The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…

Company / brand: American Contract Systems recalls

Official ID Z-3000-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline medical convenience kit labeled as recall — Medline Industries, LP

Component labeling discrepancy

Company / brand: Medline Industries recalls

Official ID Z-2999-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Onli 17cm Hydrophilic Urethral Intermittent Catheter recall — Hollister Ulc

Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to genitourinary…

Company / brand: Hollister Ulc recalls

Official ID Z-2998-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline medical convenience kits recall — Medline Industries, LP

Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…

Company / brand: Medline Industries recalls

Official ID Z-2997-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline medical convenience kits recall — Medline Industries, LP

Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…

Company / brand: Medline Industries recalls

Official ID Z-2996-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline medical convenience kits recall — Medline Industries, LP

Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…

Company / brand: Medline Industries recalls

Official ID Z-2995-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline medical convenience kits recall — Medline Industries, LP

Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…

Company / brand: Medline Industries recalls

Official ID Z-2994-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline breathing circuits labeled as recall — Medline Industries, LP

Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke,…

Company / brand: Medline Industries recalls

Official ID Z-2993-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline breathing circuits labeled as recall — Medline Industries, LP

Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke,…

Company / brand: Medline Industries recalls

Official ID Z-2992-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Medline Hudson RCI recall — Medline Industries, LP

Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke,…

Company / brand: Medline Industries recalls

Official ID Z-2991-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Philips Incisive CT with software V4 recall — Philips Healthcare (Suzhou) Co., Ltd.

Potential of failing to trigger clinical scan during Bolus Tracking.

Company / brand: Philips Healthcare (Suzhou) Co recalls

Official ID Z-2988-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICA recall — Africando Foods LLC

Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list

Company / brand: Africando Foods recalls

Official ID H-1381-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

Horizon Organic ORG ASEP CHOC MILK 1% 8OZ 12 CT (Item 136990 recall — Horizon Organic Dairy, LLC

Product has the potential to be spoiled.

Company / brand: Horizon Organic Dairy recalls

Official ID H-1333-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

Mehadrin Chocolate Leben recall — UPSTATE NIAGARA COOPERATIVE

Product may have been improperly pasteurized.

Company / brand: UPSTATE NIAGARA COOPERATIVE recalls

Official ID H-1332-2026 · Official record ↗

FDA Class I · Food · September 2, 2026

Jalapeno Ranch recall — Jaime's Foods ATX, LLC

Undeclared Egg Allergen

Company / brand: Jaime's Foods ATX recalls

Official ID H-1301-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

Byron White FORMULAS A-FNG Herbal Supplement 1 recall — Byron White Formulas, Inc.

Label does not declare walnuts in English

Company / brand: Byron White Formulas recalls

Official ID H-1278-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

Byron White FORMULAS A-P Herbal Supplement 1 recall — Byron White Formulas, Inc.

Label does not declare walnuts in English

Company / brand: Byron White Formulas recalls

Official ID H-1277-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

Byron White FORMULAS A-L Complex Herbal Supplement 1 recall — Byron White Formulas, Inc.

Label does not declare walnuts in English

Company / brand: Byron White Formulas recalls

Official ID H-1276-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with cocon recall — Lidl US TRADING

The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coco…

Company / brand: Lidl US TRADING recalls

Official ID H-1275-2026 · Official record ↗

FDA Class II · Food · September 2, 2026

ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling recall — Lidl US TRADING

The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coco…

Company / brand: Lidl US TRADING recalls

Official ID H-1274-2026 · Official record ↗

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Government sources last checked October 22, 2026 at 12:00 PM UTC.