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

24276–24300 of 26082

HighFDA (Devices)·Z-0044-2022·2021-10-13
ZOLL COOL LINE Intravascular Catheter Kit Recalled for Potential Leaks
ZOLL Circulation is recalling COOL LINE intravascular heat exchange catheters due to potential leaks in the catheter or start-up kit tubing that could affect their function during medical procedures.
Product
ZOLL, REF 8700-0781-14 (CL-2295CO), COOL LINE Intravascular Heat Exchange Catheter kit with central venous infusion capabilities (3 lumens), HEPARIN COATED, STERILE EO, Rx Only, UDI: (01)00849111075510
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0065-2022·2021-10-13
ZOLL Quattro IV therapy kit recalled due to potential catheter tubing leaks
ZOLL is recalling its Quattro IVTM Disposable Pack and Start UP Kit due to potential leaks in the catheter or tubing. The recall affects 579 bundled kits distributed worldwide.
Product
Zoll, REF 8700-000871-40, Quattro (Heparin) IVTM Disposable Pack and Start UP Kit (6 ft.), EU, New Luer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0015-2022·2021-10-13
Paltop Scan Abutment MU devices recalled for manufacturing tolerance deviations
Paltop Advanced Dental Solutions is recalling 337 Scan Abutment MU devices due to manufacturing tolerance deviations in orientation and sizing that may delay dental restoration procedures.
Product
Scan Abutment MU, Cat. No. 30-70103 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in surgica
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V794000·2021-10-13
Porsche Taycan hazard lights may activate unexpectedly
Certain 2020-2021 Porsche Taycan vehicles have hazard lights that may activate in non-emergency situations, potentially confusing drivers. Dealers will reprogram the lights at no cost.
Product
PORSCHE — 2021 PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0064-2022·2021-10-13
Zoll ICY Heparin Disposable Infusion Kits Recalled Due to Potential Leaks
ZOLL Circulation is recalling approximately 1,122 ICY Heparin infusion kits distributed worldwide due to potential leaks in the catheter or start-up kit tubing. No illnesses or injuries have been reported.
Product
Zoll, REF 8700-000870-40, ICY (Heparin) IVTM Disposable Pack and Start UP Kit (6 ft.), EU, New Luer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0004-2022·2021-10-13
Duke of Earle Ham and Cheese Sandwiches Recalled for Undeclared Allergens
The Earl of Sandwiches is recalling Duke of Earle X-Large Ham & Cheese sandwiches because they may contain undeclared soy and egg, which pose a risk to consumers with allergies to these ingredients.
Product
Duke of Earle X-Large Ham & Cheese, Ham and American Cheese on French Bread. Net Wt. 10.25 oz (297g), UPC 97256 14322, Keep Refrigerated. Earle of Sandwiches, Willernie, MN 55090
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0076-2022·2021-10-13
Cardiosave IABP helium indicator may show inaccurate readings during electromagnetic interference
Datascope Corp. is recalling Cardiosave Rescue IABP devices because the helium indicator may overrepresent the amount of helium in the unit when electromagnetic interference is present.
Product
Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0026-2022·2021-10-13
Exactech OPTETRAK Knee Implant Inserts Recalled for Inadequate Packaging
Exactech is recalling 8,985 OPTETRAK Comprehensive Knee System inserts due to insufficient oxygen barrier protection in vacuum packaging. The packaging deficiency was identified as the basis for the recall.
Product
OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0047-2022·2021-10-13
Zoll ICY intravascular heat exchange catheter kit recalled for potential leaks
ZOLL Circulation is recalling 33,066 units of the Zoll REF 8700-0782-40 ICY Intravascular Heat Exchange Catheter Kit due to potential leaks in the catheter or start-up kit tubing.
Product
Zoll REF: 8700-0782-40 (IC-3893AE), ICY Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens),HEPARIN COATED, Sterile EO, Rx Only, UDI: (01)00849111075251
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0069-2022·2021-10-13
CardioQuip Modular Cooler-Heater Units Recalled for Bacterial Water Contamination
CardioQuip heater-cooler refrigeration modules used in operating rooms could develop bacterial contamination in water systems, potentially exposing patients to infection during surgery.
Product
CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with heat exchange devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0012-2022·2021-10-13
Centricity Universal Viewer fails to save study changes to archive systems
GE Healthcare's Centricity Universal Viewer has a software defect where changes to radiological studies are not saved to archive systems, potentially affecting clinician access to current image data.
Product
Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0072-2022·2021-10-13
ARCH Leg Positioning System recalled due to locking pin engagement failure
Innovative Orthopedic Technologies is recalling the ARCH Leg Positioning System due to manufacturing defects that prevent locking pins from properly engaging under load.
Product
ARCH Leg Positioning System
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22006·2021-10-13
Specialized Tarmac SL7 Bicycles Recalled for Fork Steerer Tube Cracking Risk
Specialized Bicycle Components is recalling Tarmac SL7 bicycles and framesets because the fork steerer tube can crack or break after harsh impact, posing fall and injury hazards. About 6,900 units sold nationwide from July 2020 through August 2021 are affected.
Product
Specialized Tarmac SL7 Bicycles and Framesets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0058-2022·2021-10-13
Zoll Quattro IVTM Disposable Pack and Start UP Kit Potential Leak Hazard
ZOLL Circulation is updating product labeling for Quattro IVTM disposable packs and start-up kits due to potential leaks from catheter or tubing components. Distribution includes US nationwide and international markets.
Product
Zoll, REF 8700-000766-01, Quattro IVTM Premium Disposable Pack and Start UP Kit (6 ft.)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0028-2022·2021-10-13
FDA Recalls TECNIS Eyhance Intraocular Lenses for Elevated Endotoxin
Johnson & Johnson is recalling TECNIS Eyhance intraocular lenses due to elevated endotoxin levels exceeding internal and FDA specification limits. Affected lenses were distributed nationwide in Illinois.
Product
TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation in the capsular bag. The TECNIS Simplicity Delivery System is designed as a single-use disposable preloaded modular cartridge that functions as both the primary packaging and as a sterile, disposabl
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V793000·2021-10-12
2019-2022 Winnebago Travato and Boldt RV Electrical Fire Hazard
Winnebago is recalling 2019-2022 Travato and 2021-2022 Boldt RVs. A faulty wire harness may lose over-current protection, causing wires to overheat and increasing fire risk. Owners must not drive until the Volta Power System is disabled.
Product
WINNEBAGO — 2019 WINNEBAGO TRAVATO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V784000·2021-10-08
2021–2022 Forest River Puma travel trailers recalled for missing tank ventilation
Forest River is recalling certain 2021–2022 Puma travel trailers. The black wastewater-holding tank may lack ventilation, allowing methane gas to accumulate and increase fire risk.
Product
FOREST RIVER — 2022 FOREST RIVER PUMA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22701·2021-10-07
Joovy Zoom 360 Ultralight Jogging Strollers Recalled for Fall Hazard
Joovy is recalling about 9,200 Zoom 360 Ultralight jogging strollers because the front wheel bearing can fail or detach, creating a fall hazard. The company is offering a free repair kit.
Product
Zoom 360 Ultralight jogging strollers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V783000·2021-10-07
2022 Tiffin Phaeton Recreational Vehicle Electrical Wiring Defect
Tiffin Motorhomes is recalling certain 2021-2022 Phaeton recreational vehicles due to an electrical outlet not properly installed during manufacturing, creating an open electrical wire inside the wall that could increase the risk of fire.
Product
TIFFIN — 2022 TIFFIN PHAETON
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2582-2021·2021-10-06
Ultrasound Gel Products Recalled for Possible Bacterial Contamination
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. The FDA recommends healthcare providers stop using these products immediately.
Product
Norco Ultrasound Gel, Item/Description: NC70479/Norco Ultrasound Gel, 250 mL; NC70479/North Coast Ultrasound Gel, 250 mL; NC70479-5/Norco Ultrasound Gel, 5 liters; NC70479-5/North Coast Ultrasound Gel, 5 liters; NC70479-5C/Norco Ultrasound Gel, 5 liters (4); NC70479-5C/North Coas
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2592-2021·2021-10-06
Atrium Pneumostat Chest Drain Valve Recalled Following Fatal Preterm Infant Case
Atrium Medical Corporation is recalling 92,430 units of its Pneumostat Chest Drain Valve after a preterm infant died during treatment with the device. The company is revising product labeling and warnings.
Product
Atrium Pneumostat Chest Drain Valve, Part Number 16100
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2499-2021·2021-10-06
DeRoyal Procedure Packs with NORMOFLO Warming Sets Recalled for Aluminum Leaching
DeRoyal procedure packs containing Smiths Medical NORMOFLO warming systems are recalled due to potential aluminum ion leaching into warming fluids. The FDA classified this Class I recall affecting 2880 units distributed in Florida and South Carolina.
Product
DeRoyal Procedure Packs containing Smiths Medical NORMOFLO Irrigation Warming Set
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2518-2021·2021-10-06
FDA Recalls Ultrasound Gels for Bacterial Contamination Risk
Omnisound Gel and EcoGel 200 ultrasound gels distributed nationwide from January 2018 to August 2021 may contain bacterial contamination. The FDA issued a Class I recall; health care providers should immediately stop using these products.
Product
Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle; Manufactured by Eco-Med. For use in ultrasound procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0897-2021·2021-10-06
ceFAZolin Injectable Drug Bags Recalled for Lack of Sterility Assurance
IntegraDose Compounding Services is recalling ceFAZolin 3 G in 0.9% Sodium Chloride injectable bags due to lack of sterility assurance. The recall affects 589 bags distributed to New Hampshire, Massachusetts, and Minnesota.
Product
ceFAZolin 3 G in 0.9% Sodium Chloride, 115 mL Bag for Injection, Sterile Product, IntegraDose Compounding Services, LLC, 719 Kasota Ave SE, Minneapolis, MN. NDC: 71139-7153-1
Category
Drug
Distribution
3 states
SevereFDA (Food)·F-1017-2021·2021-10-06
Velvet Ice Cream Raspberry Fudge Cordial Recalled for Undeclared Allergen
Velvet Ice Cream Company is voluntarily recalling Velvet Ice Cream Raspberry Fudge Cordial because it contains an undeclared allergen that is not listed on the label.
Product
Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per case
Category
Food
Distribution
0 states

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