Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

11826–11850 of 27718

HighFDA (Devices)·Z-2318-2024·2024-07-17
Dental abutment recall due to incorrect product packaging and labeling
Preat Corp recalled 7 units of 9006767 Astra EV 4.8mm Milled Titanium Abutments due to incorrect products being packaged and labeled. Affected units were distributed in California, Missouri, and Nevada.
Product
9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-2310-2024·2024-07-17
Hand Procedure Kit Recalled for Excess Ethylene Oxide Residuals
American Contract Systems recalls HAND PACK-Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residuals on the cast padding component, exceeding safe permanent-contact exposure limits.
Product
HAND PACK-Procedure Kit Catalog Number: WEHD16B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2024·2024-07-17
Cast Padding Component Recalled for Excess Ethylene Oxide Residuals
American Contract Systems Inc is recalling ACL cast padding components due to ethylene oxide/ethylene chlorohydrin residuals exceeding safe limits for permanent skin contact devices. Affected product distributed nationwide.
Product
ACL, ST LUKES METHODIST 1CS Catalog Number: LMAC10AA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2273-2024·2024-07-17
ALPHAMAXX Mobile Operating Table Charger Defect Poses Equipment Failure Risk
Getinge has recalled 7 ALPHAMAXX mobile operating tables due to a defective charger unit that may not charge properly, risking equipment operational failure during use.
Product
ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322F5
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-2308-2024·2024-07-17
Knee Procedure Kit Recalled Due to Ethylene Oxide Residual Contamination
American Contract Systems Inc recalls 174 units of CUSTOM KNEE procedure kits due to ethylene oxide and ethylene chlorohydrin residuals exceeding safe exposure limits for permanent contact devices.
Product
CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AG
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2024·2024-07-17
Procedure Kit Recalled for Excess Ethylene Oxide Residue in Cast Padding
American Contract Systems Inc is recalling 36 units of Hand Pack procedure kits due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component exceeding regulatory limits.
Product
HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2281-2024·2024-07-17
Arthroscopy Procedure Tray Recalled for Sterilant Residual Contamination
American Contract Systems Inc is recalling 272 units of the ARTHROSCOPY SUP JOI PACK Procedure Tray because sterilant residuals in the cast padding exceeded safe limits for permanent implant use.
Product
ARTHROSCOPY SUP JOI PACK Procedure tray Catalog Number: BPAS17C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2278-2024·2024-07-17
Knee surgery procedure tray recalled for chemical contamination
American Contract Systems is recalling TOTAL KNEE procedure trays (Catalog Number BFTK01AA) due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component that exceed acceptable regulatory limits.
Product
TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2280-2024·2024-07-17
Arthroscopy Procedure Tray Recalled for Excess Sterilization Residue
American Contract Systems recalls the ARTHROSCOPY WOLFSON PACK BHS Procedure tray because ethylene oxide residuals on the cast padding exceeded safety limits for permanent exposure medical devices.
Product
ARTHROSCOPY WOLFSON PACK BHS Procedure tray Catalog Number: BPAR65A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2302-2024·2024-07-17
Medical knee procedure kit recalled for excessive sterilization chemical residue
American Contract Systems Inc is recalling TOTAL KNEE-Procedure Kits due to excessive ethylene oxide and ethylene chlorohydrin residues on the cast padding component. The recall affects 85 units distributed nationwide.
Product
TOTAL KNEE-Procedure Kit Catalog Number: SMTK21C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2324-2024·2024-07-17
ZOLL Powerheart G5 AED shipping film may prevent shock delivery
ZOLL Powerheart G5 AED devices are shipped with a protective film on the front panel. If not removed before use, the film may prevent the shock button from being pressed, delaying or preventing defibrillation therapy.
Product
ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA). Model/Catalog Number: G5S-00A G5S-0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2285-2024·2024-07-17
Foot-Ankle Procedure Tray Recalled for Excessive Sterilization Residue
American Contract Systems Inc is recalling 107 units of FOOT ANKLE-LF Procedure tray distributed nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safety limits for permanent-implant devices.
Product
FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0590-2024·2024-07-17
Bupropion Extended-Release Tablets Recalled for Dissolution Failure
Amerisource Health Services is recalling Bupropion Hydrochloride 150mg extended-release tablets nationwide due to dissolution specification failures. The tablets dissolve faster than specified limits.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2344-2024·2024-07-17
Blood Pump Rotor Spare Part Recall Due to Loose Guide Sheaves
Fresenius is recalling 17 Blood Pump Rotor spare parts nationwide due to loose or dislodged guide sheaves that develop after use. The affected rotor components are used in K@HOME dialysis machines.
Product
RTL190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2333-2024·2024-07-17
Ophthalmic Injection Kit Recall Due to Unconfirmed Sterilization
MICROspecialties is recalling the Synergetics I Pack Injection Kit because sterilization cannot be confirmed, potentially causing post-operative wound or injection site infections. Affected units are lot P62764979R distributed in Missouri.
Product
Synergetics I Pack Injection Kit- Tray for use with Ophthalmic injections Model/Catalog Number: 18060
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2334-2024·2024-07-17
Medical Injection Kit Recall Due to Unconfirmed Sterilization
MICROspecialties is recalling Synergetics I-Pack Injection Kits because some units may not have been properly sterilized, potentially causing post-operative wound or injection site infections.
Product
Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injections Model/Catalog Number: 18061
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2341-2024·2024-07-17
Blood Pump Rotor Guide Sheaves May Loosen in Home Hemodialysis System
Fresenius is recalling Blood Pump Rotor components in 2008K@HOME hemodialysis systems due to reports of loose or dislodged guide sheaves that could affect pump function. Affected patients should contact their clinic to verify involvement.
Product
190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2299-2024·2024-07-17
TOTAL KNEE-Procedure Kit Recalled Due to Ethylene Oxide Residuals
American Contract Systems is recalling 976 units of TOTAL KNEE-Procedure Kits nationwide due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component that exceed safe exposure limits for medical devices.
Product
TOTAL KNEE-Procedure Kit Catalog Number: SFTK54B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2317-2024·2024-07-17
GE Vivid Ultrasound Scanner Displays Incorrect Patient Data
GE Vivid ultrasound systems may display incorrect patient names and demographics due to slow DICOM response times, risking patient misidentification during imaging.
Product
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-2270-2024·2024-07-17
24K Premium Contact Lenses Recalled Due to Potential Bacterial Contamination
Ontact Inc. is recalling 24K Premium contact lenses distributed in California and Nevada due to potential bacterial contamination.
Product
24K Premium Lense, Distributed by Updream Inc.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2291-2024·2024-07-17
Knee Arthroscopy Pack Recalled for Excess Sterilization Residues
American Contract Systems Inc. is recalling 84 knee arthroscopy packs (Catalog Number MEKA12R) distributed nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safe limits for permanent exposure medical devices.
Product
KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2330-2024·2024-07-17
Presource Neurological Surgical Kits Recalled for Syringe Design Defect
Cardinal Health is recalling Presource neurological surgical kits containing defectively designed syringes that may cause inaccurate dosing or device leakage. The recall affects 13,487 kits distributed nationwide.
Product
Presource kits and trays, labeled as: 1) Neurological Tray, Catalog Number SAN29NICCA; 2) Neurological Tray, Catalog Number SAN29NRCC1; 3) Neurological Tray, Catalog Number SAN29NRCC2; 4) Neurological Tray, Catalog Number SAN29NRCC3; 5) Neurological Tray, Catalog Number SAN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2301-2024·2024-07-17
Surgical Knee Arthroscopy Kit Recalled for Excessive Sterilization Gas Residuals
American Contract Systems Inc is recalling its KNEE ARTHROSCOPY-Procedure Kit nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safe limits for permanent medical devices. The recall affects 28 units with lot numbers 975241 and 920241.
Product
KNEE ARTHROSCOPY-Procedure Kit Catalog Number: SLAR14G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2335-2024·2024-07-17
Ophthalmic injection kit recalled over sterilization confirmation failure
MICROspecialties recalls 780 units of the Synergetics I Pack Injection Kit (Model 18069) because the company could not confirm proper sterilization, creating risk of post-operative or injection-site infections.
Product
Synergetics I Pack Injection Kit Custom-Tray for use with Ophthalmic injections Model/Catalog Number: 18069 Product Description:
Category
Medical Device
Distribution
1 state
HighFDA (Food)·F-1475-2024·2024-07-17
Food recall: Bakeshop muffins contain undeclared walnut allergen
Bakeshop Chocolate Chip Muffins sold at ALDI stores nationwide are being recalled because they contain undeclared walnut, a common allergen. Consumers with walnut allergies should not consume the product.
Product
Bakeshop Chocolate Chip Muffin 4 count, in clear plastic clamshell, UPC 4099100048278. 5 retail units per case.
Category
Food
Distribution
Distributed nationwide

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11826–11850 of 27718