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

4976–5000 of 27364

HighFDA (Devices)·Z-2329-2024·2024-07-17
Cardiovascular Procedure Kits Recalled for Potential Syringe Design Defects
Cardinal Health recalls 17,445 cardiovascular procedure kits nationwide containing potentially defective syringes that could cause inaccurate dosing or device leakage.
Product
Presource kits and trays, labeled as: 1) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC3; 2) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC4; 3) Cardiovascular Procedure Kit, Catalog Number SAN29ANCCL; 4) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2284-2024·2024-07-17
Medical Device Procedure Tray Recalled for Excessive Sterilant Chemical Residue
American Contract Systems Inc is recalling the BPKN15C Knee Basin Pack procedure tray because sterilant residues (ethylene oxide and ethylene chlorohydrin) exceed safe limits for permanent-use medical devices.
Product
BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C
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-2286-2024·2024-07-17
Procedure Tray Recalled Due to Excess Sterilization Residue
American Contract Systems Inc is recalling HAND WRIST FOREARM-LF Procedure trays due to ethylene oxide sterilization residues exceeding safe limits for permanent exposure devices.
Product
HAND WRIST FOREARM-LF Procedure tray Catalog Number: CCHD17B
Category
Medical Device
Distribution
Distributed nationwide
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-2282-2024·2024-07-17
Procedure Tray Recalled for Excessive Ethylene Oxide Residuals
American Contract Systems Inc is recalling 129 units of ARTHO KNEE BAPTIST SOUTH PACK Procedure trays (lot numbers 953241, 882241) due to ethylene oxide and ethylene chlorohydrin sterilization residuals exceeding safe limits for permanent-contact medical devices.
Product
ARTHO KNEE BAPTIST SOUTH PACK Procedure tray Catalog Number: BPKA49B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2283-2024·2024-07-17
Orthopedic knee procedure tray recalled for sterilization residue levels
American Contract Systems Inc is recalling 84 units of the ARTHRO KNEE BEACHES PACK BHS procedure tray because residual sterilization chemicals exceeded permissible exposure limits. The affected units were distributed nationwide.
Product
ARTHRO KNEE BEACHES PACK BHS- Procedure tray Catalog Number: BPKB46B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2347-2024·2024-07-17
Blood Pump Rotor Spare Parts Recalled for Loose Guide Sheaves
Fresenius Medical Care recalls 6 blood pump rotor spare parts used in dialysis machines due to loose or dislodged guide sheaves that developed after clinical use.
Product
RTLR190395: 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-2298-2024·2024-07-17
Knee Arthroscopy Kit Recalled for Excessive Sterilant Chemical Residue
American Contract Systems Inc is recalling 270 units of a knee arthroscopy surgical kit because sterilization chemical residues exceed safe limits for permanent device contact.
Product
KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2337-2024·2024-07-17
Endoscopic Vessel Harvesting System Recalled for Altered Component Spacing
Maquet Cardiovascular is recalling 600 units of the VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System due to reports of C-Ring wire straightening and altered spacing between components. No adverse events have been reported.
Product
The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2311-2024·2024-07-17
Hand Pack Procedure Kit recalled for excess ethylene oxide residuals
American Contract Systems Inc is recalling the HAND PACK-Procedure Kit (catalog WEHD16C) due to ethylene oxide and ethylene chlorohydrin residuals exceeding safety limits.
Product
HAND PACK-Procedure Kit Catalog Number: WEHD16C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2306-2024·2024-07-17
Surgical Procedure Kit Recalled for Ethylene Oxide Residual Contamination
American Contract Systems Inc is recalling the ACL PACK Surgical Procedure Kit due to elevated ethylene oxide and ethylene chlorohydrin residuals that exceed regulatory limits for permanent-contact medical devices.
Product
ACL PACK - 206039-Procedure Kit Catalog Number: UDAC66AA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2307-2024·2024-07-17
CUSTOM KNEE Medical Device Procedure Kit recalled for excess chemical residuals
American Contract Systems Inc is recalling 174 units of the CUSTOM KNEE - 206061-Procedure Kit due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component. The residuals exceed the safety limits specified in ANSI/AAMI/ISO 10993-7:(R)2012 for permanent-contact medical devices.
Product
CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2288-2024·2024-07-17
Upper Extremity Cast Padding Recalled for Excessive Sterilization Gas Residuals
American Contract Systems Inc. is recalling 192 units of cast padding due to excessive ethylene oxide and ethylene chlorohydrin residuals exceeding safe limits for skin-contact medical devices.
Product
UPPER EXTREMITY PK, STRL F G Catalog Number: IHUE40AG
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2024·2024-07-17
Arthroscopy Procedure Kit Recalled Due to Ethylene Oxide Residue
American Contract Systems Inc is recalling 27 arthroscopy procedure kits because ethylene oxide and ethylene chlorohydrin residuals in the cast padding exceeded safe exposure limits for permanent implants.
Product
ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22V
Category
Medical Device
Distribution
Distributed nationwide
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-2316-2024·2024-07-17
GE Vivid Ultrasound Systems Display Incorrect Patient Names
GE Vivid ultrasound systems may display incorrect patient information due to slow DICOM response times. Seven affected units were distributed to healthcare facilities in IL, MA, NM, NY, and OK.
Product
GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-2320-2024·2024-07-17
Medical examination gloves recalled for skin irritation and disintegration
SVS LLC is recalling 155,540 boxes of non-sterile nitrile examination gloves due to reported skin irritation, glove disintegration with certain cleaning solutions, and size mislabeling. Gloves were distributed nationwide across eight U.S. states.
Product
Non-sterile, single use, disposable gloves intended for medical purposes to be worn on the hands of examiners to prevent contamination between a patient and an examiner. The gloves are nitrile, powder-free, ambidextrous, and blue-colored with a beaded cuff. The range of sizes inc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2271-2024·2024-07-17
ALPHAMAXX Operating Table Defective Charger Recalled for Operational Failure Risk
Getinge Usa Sales Inc recalls 73 ALPHAMAXX mobile operating tables due to a defective charger unit that poses a risk of inadequate charging and operational failure.
Product
ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4
Category
Medical Device
Distribution
4 states
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-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-2292-2024·2024-07-17
Knee Arthroscopy Procedure Kit Recalled for Sterilization Chemical Residue
American Contract Systems Inc is recalling 36 units of its knee arthroscopy procedure kit due to excessive sterilization chemical residues in the cast padding component that exceed safe exposure limits.
Product
KNEE ARTHROSCOPY-Procedure Kit Catalog Number: QPKA35A
Category
Medical Device
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-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-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

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4976–5000 of 27364