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

23901–23925 of 26082

HighFDA (Devices)·Z-0213-2022·2021-11-17
Philips Azurion X-Ray Systems may lock up during simultaneous button presses
Philips Azurion Interventional X-Ray Systems (software 2.1.x) may experience imaging lock-up when operators simultaneously press both the APC and Float Tabletop buttons.
Product
Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228. (Azurion 3 M12, Azurion 3 M15, Azurion 5 M12, Azurion 5 M20, Azurion 7
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0168-2022·2021-11-17
Testosterone Bi-Blend Injectable Recalled for Lack of Sterility Assurance
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Testosterone Bi-Blend 100/100 mg/mL injectable due to lack of assurance of sterility. The product was distributed across the United States, including Washington, D.C. and Puerto Rico.
Product
TESTOSTERONE BI-BLEND 100/100MG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
Category
Drug
Distribution
0 states
HighFDA (Food)·F-0129-2022·2021-11-17
E-Z Spuds Green Pepper Julienne Recalled for Salmonella Risk
E-Z Spuds Inc. is recalling 25-pound cases of Green Pepper Julienne due to potential Salmonella contamination. The affected product was distributed to manufacturers and food service establishments in the Chicago, Illinois metro area.
Product
E-Z Spuds Inc. 25# Green Pepper Julienne 1/4"
Category
Food
Distribution
1 state
HighFDA (Food)·F-0152-2022·2021-11-17
Country Oven Boston Cream Cake recalled for possible metal fragments
The Kroger Co is recalling Country Oven Boston Cream Cake Double Layer Cake (28 oz) due to possible metal fragments in starch used in manufacturing. The product was distributed across multiple states with a use-by date of 04/04/22.
Product
Country Oven Boston Cream Cake Double Layer Cake 28oz
Category
Food
Distribution
29 states
HighFDA (Food)·F-0153-2022·2021-11-17
Country Oven Raspberry Cake recalled for possible metal fragments
The Kroger Co. is recalling Country Oven Raspberry Cake (71 oz, UPC 0001111006321, Use By 003/21/22) distributed across 28 states due to possible metal fragments in starch used during manufacturing.
Product
Country Oven Raspberry Cake 71oz
Category
Food
Distribution
29 states
HighFDA (Drugs)·D-0104-2022·2021-11-17
Alprostadil Injectable Recalled for Lack of Sterility Assurance
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Alprostadil 40 mcg/mL injectable vials due to lack of assurance of sterility. The recall affects the U.S. including Washington, D.C. and Puerto Rico.
Product
ALPROSTADIL 40MCG/ML INJ 40MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
Category
Drug
Distribution
0 states
HighFDA (Drugs)·D-0099-2022·2021-11-17
Alprostadil Injectable Recalled for Lack of Sterility Assurance
Vita Pharmacy, LLC dba Talon Compounding Pharmacy is recalling Alprostadil 22.5mcg/mL Injectable due to lack of assurance of sterility. The affected lot was distributed across the United States, including Washington, D.C. and Puerto Rico.
Product
ALPROSTADIL 22.5MCG/ML 22.5MCG/ML INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
Category
Drug
Distribution
0 states
HighFDA (Food)·F-0132-2022·2021-11-17
E-Z Spuds Inc. Diced Celery Recall for Potential Salmonella
E-Z Spuds Inc. is recalling diced celery products due to potential Salmonella contamination. The affected products were distributed to manufacturers and food service establishments in the Chicago, IL metro area.
Product
E-Z Spuds Inc. 10# 30# Celery diced, crosscut
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0215-2022·2021-11-17
Hemodialysis Delivery System Software May Use Incorrect Treatment Parameters
Baxter's Hemodialysis Delivery System may incorrectly revert to old prescription values when operators change prescriptions after filter changes, potentially resulting in incorrect treatment parameters.
Product
Hemodialysis Delivery System, Software Version 2.x.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0126-2022·2021-11-17
E-Z Spuds Inc. Parsley Crosscut Potatoes Recalled for Salmonella Risk
E-Z Spuds Inc. is recalling 60 cases of 10# Parsley Crosscut 1/4" potatoes distributed to manufacturers and food service establishments in the Chicago, IL metro area due to potential Salmonella contamination.
Product
E-Z Spuds Inc. 10# Parsley Crosscut 1/4"
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0212-2022·2021-11-17
Photopheresis Kit Recalled Due to Incomplete Testing Before Release
Therakos is recalling 15 photopheresis kits because they were released before testing was completed. If used, a drive tube leak could cause illness or injury.
Product
THERAKOS CELLEX Photopheresis Procedural Kit PRODUCT CODE: CLXUSA
Category
Medical Device
Distribution
1 state
HighFDA (Food)·F-0141-2022·2021-11-17
Country Oven Chocolate/Vanilla Cake Recalled for Metal Fragment Risk
The Kroger Co is recalling Country Oven Chocolate/Vanilla Cake (37 oz) due to possible metal fragments in the starch used to manufacture the cakes. The product was distributed across 28 states.
Product
Country Oven Chocolate/Vanilla Cake 37oz
Category
Food
Distribution
29 states
HighNHTSA·21V885000·2021-11-16
2021 Entegra Cornerstone Motorhome Power Steering Pump Defect Recall
Jayco recalls certain 2021 Entegra Cornerstone motorhomes with a power steering pump defect that may result in loss of steering assist. Owners should contact Jayco for free pump replacement to prevent increased crash risk.
Product
ENTEGRA — 2021 ENTEGRA CORNERSTONE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V878000·2021-11-12
Alfa Romeo Stelvio and Giulia fuel line sensor housing cracks
The fuel line sensor housing in certain 2020-2021 Alfa Romeo Stelvio and Giulia vehicles may crack and leak fuel, causing engine stalls and increasing fire risk.
Product
ALFA ROMEO — 2020 ALFA ROMEO STELVIO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V876000·2021-11-12
2021-2022 Continental Cargo and Cargo Mate Trailers: Welding Defect in Coupler
Forest River is recalling certain 2021-2022 Continental and Cargo Mate cargo trailers due to an improperly welded coupler. The defect may cause the trailer to separate from the tow vehicle, increasing crash risk.
Product
CONTINENTAL CARGO — 2021 CONTINENTAL CARGO CARGO TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V877000·2021-11-12
2021-2022 Forest River Cherokee Travel Trailers Recalled for Incorrect Tire Placard
Forest River is recalling 2021-2022 Cherokee travel trailers because the tire size and weight rating printed on the Federal Placard are incorrect. This could cause the vehicle to be overloaded and lose control.
Product
FOREST RIVER — 2021 FOREST RIVER CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22707·2021-11-12
RH Lambeth Outdoor Metal Torches Recalled for Fire Hazard
RH is recalling about 1,200 Lambeth outdoor metal torches because fuel can leak from the canister top and ignite, creating a fire hazard. No injuries have been reported. Consumers should stop using the torches and contact RH for a refund.
Product
Lambeth Outdoor Metal Torches
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0119-2022·2021-11-10
Monoject Prefilled Syringe Plunger Defect Recall: Air Reintroduction Risk
Monoject prefilled syringes in medical kits may have a plunger that rebounds after air expulsion, potentially reintroducing air into the syringe. This FDA Class I recall affects approximately 9,378 units distributed in Florida and Pennsylvania.
Product
Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 8881570121 inside the following Aligned Medical Solutions Custom Convenience Kits: AMS-9041CP Leaderflex Insertion Kit with Ultrasound, AMS-9046CP-1 Insertion Tray-RX, AMS8939A Universal Procedure Pack w/Sp
Category
Medical Device
Distribution
2 states
SevereFDA (Drugs)·D-0093-2022·2021-11-10
Cubicin daptomycin injection recalled for glass particle contamination
Merck Sharp & Dohme Corp. is recalling Cubicin (daptomycin for injection) 500 mg vials due to the presence of glass particles. The recall affects a single lot distributed nationwide.
Product
Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V873000·2021-11-10
Jeep Wagoneer and Grand Cherokee Airbag Control Software Defect
The Occupant Restraint Controller software in certain 2021-2022 Jeep models may be faulty, allowing airbags to disable without warning. This increases crash injury risk.
Product
JEEP — 2022 JEEP WAGONEER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0090-2022·2021-11-10
Lupin Pharmaceuticals Irbesartan/Hydrochlorothiazide Tablets Recalled for Impurity
Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets USP (300/12.5 mg) in 30-count and 90-count bottles due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient.
Product
Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0114-2022·2021-11-10
Green Giant Fresh Whole Yellow Onions Recalled for Salmonella Risk
POTANDON PRODUCE LLC is recalling Green Giant Fresh whole yellow onions sold in 2 lb., 3 lb., and 5 lb. bags due to potential Salmonella Oranienburg contamination. The product was distributed in North Dakota and Minnesota.
Product
Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg. per case) - UPC 60580600120-8. Green Giant Fresh whole YELLOW onions in 3 lbs. flexible mesh bags, (16/3 lb. pkg. per case) - UPC 60580600123-9. Green Giant Fresh whole YELLOW onions in 5 lbs. fl
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-0092-2022·2021-11-10
Methocarbamol Tablets Mislabeled with Incorrect Strength
Bryant Ranch Prepack is recalling Methocarbamol 500mg tablets nationwide because the bottles are mislabeled—they actually contain 750mg tablets. The affected lot was distributed in 30-, 60-, and 90-count bottles.
Product
Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V872000·2021-11-10
Maserati Vehicles Recall: Fuel Line Sensor Housing May Crack and Leak
Maserati is recalling certain 2021-2022 model-year vehicles due to a defective fuel line sensor housing that may crack and leak fuel. The leak can cause engine stall or fire, increasing crash risk.
Product
MASERATI — 2022 MASERATI MC20
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0089-2022·2021-11-10
Irbesartan and Hydrochlorothiazide Tablets Recalled for Impurity Contamination
Lupin Pharmaceuticals is recalling Irbesartan and Hydrochlorothiazide Tablets 150/12.5 mg due to detection of the impurity N-nitrosoirbesartan in the active pharmaceutical ingredient, which resulted from CGMP deviations.
Product
Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only
Category
Drug
Distribution
Distributed nationwide

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23901–23925 of 26082