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

11776–11800 of 27718

SevereFDA (Devices)·Z-2313-2024·2024-07-17
Baxter VidiaPort and Trulight surgical lights recalled for thermal burn risk
Baxter Healthcare Corporation is recalling VidiaPort and Trulight surgical light systems due to customer reports of thermal skin injuries. Approximately 275 units were distributed worldwide.
Product
VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b) 4028210 (Ceiling Duo Surgical Lights); c) 4028310 (Ceiling Trio Surgical Lights)
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-1466-2024·2024-07-17
Queso Rico La Hacienda Queso Fresco Cheese Recalled for Listeria
Queso Rico La Hacienda brand queso fresco cheese was found to contain Listeria monocytogenes. FDA Class I recall affects 640 pounds distributed to retail stores in Texas counties.
Product
Queso Rico La Hacienda brand queso fresco cheese packaged in 9 oz, 1 pound, and 2 pound plastic packages. Product labeling reads in part "***QUESO RICO LA HACIENDA***EL QUESO FRESCO FRESCO DE VERACRUZ***Lic. Permit #483709 El Queso Rico "LA HACIENDA"***5617 E. Trenton Rd., Suite
Category
Food
Distribution
0 states
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-2300-2024·2024-07-17
Hand Draping Surgical Kit Recalled for Ethylene Oxide Residue
American Contract Systems Inc is recalling the Hand Draping SJH-Procedure Kit because residual levels of ethylene oxide and ethylene chlorohydrin exceeded safe limits for permanent-contact medical devices.
Product
HAND DRAPING SJH-Procedure Kit Catalog Number: SJHD67F
Category
Medical Device
Distribution
Distributed nationwide
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-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-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-2338-2024·2024-07-17
Endoscopic Vessel Harvesting System Recalled for C-Ring Wire Straightening
Maquet Cardiovascular recalled 2,463 VASOVIEW HEMOPRO 2 surgical systems due to C-Ring wire straightening and component misalignment affecting tool positioning. No injuries have been reported.
Product
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System 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-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-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-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-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-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-2277-2024·2024-07-17
Procedure Tray Recalled for Excess Ethylene Oxide Residue
American Contract Systems is recalling a lower extremity procedure tray (48 units) due to ethylene oxide residuals that exceed FDA safety limits for permanent exposure medical devices.
Product
LOWER EXTREMITY - 247542- Procedure tray Catalog Number: BFLE56X
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-2323-2024·2024-07-17
Welch Allyn CP150 Electrocardiograph recalled for missing electromagnetic interference absorber
Baxter Healthcare is recalling the Welch Allyn CP150 Electrocardiograph because a critical manufacturing step—installation of an electromagnetic interference absorber—was omitted. This could cause device malfunction or interference with nearby medical equipment.
Product
Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one of the tools that clinicians use to evaluate, diagnose, and monitor patient cardiac function.
Category
Medical Device
Distribution
0 states
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-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-2297-2024·2024-07-17
Total Knee Procedure Kit Recalled for Excess Ethylene Oxide Residue
American Contract Systems Inc is recalling a knee surgery procedure kit (24 units, Lot 939241) due to ethylene oxide sterilization residues in the cast padding exceeding safety exposure limits for permanent-implant devices.
Product
TOTAL KNEE - 297835 -Procedure Kit Catalog Number: RGTK10L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2309-2024·2024-07-17
Orthopedic ORIF Hip Rod Procedure Kit Recalled for Sterilization Residuals
American Contract Systems Inc is recalling its ORIF HIP IM RODDING FEMUR-Procedure Kit (28 units) because ethylene oxide and ethylene chlorohydrin residuals in the cast padding exceeded safe limits for permanent implants.
Product
ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2312-2024·2024-07-17
Knee Arthroscopy Kit Recalled for Elevated Sterilization Chemical Residues
American Contract Systems Inc is recalling 60 units of the KNEE ARTHROSCOPY PACK-Procedure Kit nationwide due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component exceeding established safety limits.
Product
KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B
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-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

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11776–11800 of 27718