Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,801–1,900, newest first.
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2629-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2628-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2627-2026 · Official record ↗
Potential sterile breach of the pouches in which devices are packaged.
Company / brand: Boston Scientific recalls
Official ID Z-2626-2026 · Official record ↗
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by…
Company / brand: Hamilton Medical AG recalls
Official ID Z-2625-2026 · Official record ↗
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedur…
Company / brand: Medtronic Heart Valves Division recalls
Official ID Z-2624-2026 · Official record ↗
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
Company / brand: Remel recalls
Official ID Z-2623-2026 · Official record ↗
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …
Company / brand: Windstone Medical Packaging recalls
Official ID Z-2622-2026 · Official record ↗
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …
Company / brand: Windstone Medical Packaging recalls
Official ID Z-2621-2026 · Official record ↗
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …
Company / brand: Windstone Medical Packaging recalls
Official ID Z-2620-2026 · Official record ↗
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization …
Company / brand: Windstone Medical Packaging recalls
Official ID Z-2619-2026 · Official record ↗
Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are posit…
Company / brand: Medacta Usa recalls
Official ID Z-2618-2026 · Official record ↗
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-2617-2026 · Official record ↗
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-2616-2026 · Official record ↗
Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surface…
Company / brand: Medline Industries recalls
Official ID Z-2615-2026 · Official record ↗
A single lot of expired syringes were distributed due to a distribution system control failure.
Company / brand: Mentor Texas LP recalls
Official ID Z-2614-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2613-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2612-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2611-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2610-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2609-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2608-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2607-2026 · Official record ↗
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on th…
Company / brand: Medline Industries recalls
Official ID Z-2606-2026 · Official record ↗
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The p…
Company / brand: Insulet recalls
Official ID Z-2605-2026 · Official record ↗
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The p…
Company / brand: Insulet recalls
Official ID Z-2604-2026 · Official record ↗
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The p…
Company / brand: Insulet recalls
Official ID Z-2603-2026 · Official record ↗
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the p…
Company / brand: Baxter Healthcare recalls
Official ID Z-2551-2026 · Official record ↗
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the p…
Company / brand: Baxter Healthcare recalls
Official ID Z-2550-2026 · Official record ↗
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the p…
Company / brand: Baxter Healthcare recalls
Official ID Z-2549-2026 · Official record ↗
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the p…
Company / brand: Baxter Healthcare recalls
Official ID Z-2548-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2547-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2546-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2545-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2544-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2543-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2542-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2541-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2540-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2539-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2538-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2537-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2536-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2535-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2534-2026 · Official record ↗
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…
Company / brand: Medline Industries recalls
Official ID Z-2533-2026 · Official record ↗
Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which will result in "exhalati…
Company / brand: Hamilton Medical AG recalls
Official ID Z-2463-2026 · Official record ↗
Elevated coliforms
Company / brand: Wells Enterprises recalls
Official ID H-1151-2026 · Official record ↗
Product may be contaminated with Clostridium botulinum.
Company / brand: NARA ORGANICS recalls
Official ID H-1137-2026 · Official record ↗
Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)
Company / brand: Fry Pie Factory recalls
Official ID H-1136-2026 · Official record ↗
Dietary supplement product Vista MAX contains undeclared Yellow#5.
Company / brand: Provision Health dba PH Labs recalls
Official ID H-1135-2026 · Official record ↗
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
Company / brand: Provision Health dba PH Labs recalls
Official ID H-1134-2026 · Official record ↗
Potential contamination with plastic material
Company / brand: MARS SNACKING recalls
Official ID H-1130-2026 · Official record ↗
Potential contamination with plastic material
Company / brand: MARS SNACKING recalls
Official ID H-1129-2026 · Official record ↗
Product may be contaminated with Salmonella Typhimurium
Company / brand: MOGO Moringa recalls
Official ID H-1128-2026 · Official record ↗
Undeclared peanuts.
Company / brand: Western Mixers Produce & Nuts recalls
Official ID H-1125-2026 · Official record ↗
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Company / brand: Lupin Pharmaceuticals recalls
Official ID D-0723-2026 · Official record ↗
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.
Company / brand: McKesson recalls
Official ID D-0714-2026 · Official record ↗
CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated
Company / brand: Blaine Labs recalls
Official ID D-0699-2026 · Official record ↗
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Company / brand: Blaine Labs recalls
Official ID D-0698-2026 · Official record ↗
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Company / brand: Blaine Labs recalls
Official ID D-0697-2026 · Official record ↗
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Company / brand: Blaine Labs recalls
Official ID D-0696-2026 · Official record ↗
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Company / brand: Blaine Labs recalls
Official ID D-0695-2026 · Official record ↗
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Company / brand: Blaine Labs recalls
Official ID D-0694-2026 · Official record ↗
CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated
Company / brand: Blaine Labs recalls
Official ID D-0693-2026 · Official record ↗
Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp
Company / brand: Blaine Labs recalls
Official ID D-0692-2026 · Official record ↗
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Company / brand: Cipla USA recalls
Official ID D-0676-2026 · Official record ↗
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Company / brand: Cipla USA recalls
Official ID D-0675-2026 · Official record ↗
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Company / brand: Cipla USA recalls
Official ID D-0661-2026 · Official record ↗
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
Company / brand: Lannett Company recalls
Official ID D-0660-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Asclemed USA recalls
Official ID D-0659-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Asclemed USA recalls
Official ID D-0658-2026 · Official record ↗
CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper that had previously been used for a different product.
Company / brand: Boehringer Ingelheim Pharmaceuticals recalls
Official ID D-0657-2026 · Official record ↗
Subpotent Drug
Company / brand: ACCORD HEALTHCARE recalls
Official ID D-0656-2026 · Official record ↗
Presence of Foreign Substance
Company / brand: Lupin Pharmaceuticals recalls
Official ID D-0655-2026 · Official record ↗
Failed Impurities/Degradation Specifications
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0654-2026 · Official record ↗
Lack of assurance of Sterility:
Company / brand: ACCORD BIOPHARMA recalls
Official ID D-0653-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0652-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0651-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0650-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0649-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0648-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0647-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0646-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0645-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0644-2026 · Official record ↗
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of th…
Company / brand: CareFusion 213 recalls
Official ID D-0643-2026 · Official record ↗
A noncompliant vehicle may have reduced occupant protections, increasing the risk of injury during a crash.
Company / brand: Tesla recalls
Official ID 26V445000 · Official record ↗
An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.
Company / brand: Subaru recalls
Official ID 26V436000 · Official record ↗
Steps that detach while in use increase the risk of injury. Additionally, steps that detach while in transit increase the risk of a crash.
Company / brand: Wabash National recalls
Official ID 26V435000 · Official record ↗
A fuel leak increases the risk of fire.
Company / brand: Braun recalls
Official ID 26V434000 · Official record ↗
Improper illumination from the towing lights can reduce trailer visibility to other drivers, increasing the risk of a crash.
Company / brand: Harbor Freight Tools recalls
Official ID 26E043000 · Official record ↗
An incorrect load carrying capacity modification label may lead to improper loading of the vehicle, increasing the risk of a crash.
Company / brand: Southeast Toyota Distributors recalls
Official ID 26V433000 · Official record ↗
An unsecured wheelchair can move during transit, increasing the risk of injury.
Company / brand: Prime-Time Specialty Vehicles recalls
Official ID 26E042000 · Official record ↗
A fire increases the risk of injury.
Company / brand: Hyundai Motor America recalls
Official ID 26V432000 · Official record ↗
A fire increases the risk of injury.
Company / brand: Kia America recalls
Official ID 26V431000 · Official record ↗
A fire increases the risk of injury.
Company / brand: Kia America recalls
Official ID 26V430000 · Official record ↗
A short may cause the inverter AC wiring to overheat, increasing the risk of a fire.
Company / brand: Altec Industries recalls
Official ID 26V429000 · Official record ↗
A fuel leak increases the risk of a fire.
Company / brand: Crestline Coach recalls
Official ID 26V428000 · Official record ↗
The electrical system may overheat without a ground, increasing the risk of a fire. There is also an increased risk of injury from electrical shock.
Company / brand: Jayco recalls
Official ID 26V427000 · Official record ↗
Found something wrong or missing? Report a data error.
Government sources last checked October 22, 2026 at 12:00 PM UTC.