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

1801–1825 of 5047

HighFDA (Drugs)·D-0255-2024·2024-01-24
Secret Dry Spray Antiperspirant Recalled Due to Manufacturing Facility Contamination Risk
The FDA is recalling certain lots of Secret Dry Spray Antiperspirant due to a manufacturing facility deviation and potential benzene contamination. All affected lots expire through September 2023.
Product
Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0253-2024·2024-01-24
Secret anti-perspirant spray recalled for potential benzene contamination
The FDA is recalling Secret powder fresh anti-perspirant spray due to potential benzene contamination found at the manufacturing facility.
Product
Secret, powder fresh, (Aluminum chlorohydrate 24%), Anti-Perspirant/Deodorant, Topical spray can Net Wt., (a) 4OZ (113g), NDC 37000-134-11, UPC 0 37000 71109 4, (b) 6OZ (170g), NDC 37000-134-17, UPC 0 37000 71108 7; (c) twin pack-2 Topical spray cans, each can Net Wt. 6OZ (170g)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0231-2024·2024-01-24
Magnesium Citrate Oral Solution Recalled for Bacterial Contamination
Pharma Nobis LLC is recalling 7,404 bottles of Freskaro Magnesium Citrate Oral Solution nationwide due to the presence of Acetobacter nitrogenifigens bacteria.
Product
MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - CHERRY)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0228-2024·2024-01-24
Walgreens Dye-Free Magnesium Citrate Saline Laxative Recalled for Bacterial Contamination
Walgreens Dye-Free Magnesium Citrate Saline Laxative is being recalled nationwide due to bacterial contamination. The FDA identified Acetobacter nitrogenifigens in the product.
Product
MAGNESIUM CITRATE — MAGNESIUM CITRATE (MAGNESIUM CITRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0230-2024·2024-01-24
Freskaro Magnesium Citrate oral solution recalled for bacterial contamination
Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Grape Flavor) nationwide due to the presence of Acetobacter nitrogenifigens bacteria.
Product
MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0220-2024·2024-01-17
Prescription Vigabatrin Powder Recalled for Defective Container Leakage Risk
InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.
Product
VIGABATRIN — VIGABATRIN (VIGABATRIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0222-2024·2024-01-17
FDA recalls Bupropion Hydrochloride tablets for foreign tablet contamination
Rising Pharma Holdings is recalling 47,976 bottles of Bupropion Hydrochloride 150mg tablets nationwide due to foreign tablets or capsules found in some bottles. Consumers should stop use and contact their pharmacist immediately.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0219-2024·2024-01-17
Prescription Tacrolimus Capsules Recalled for Wrong-Strength Product Mix
Dr. Reddy's Laboratories is recalling 8,280 bottles of Tacrolimus 1 mg capsules after a 0.5 mg capsule was found in a bottle. The wrong-strength capsule could cause dosage confusion.
Product
TACROLIMUS — TACROLIMUS (TACROLIMUS)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0221-2024·2024-01-17
FDA Recalls Desloratadine Tablets Due to Manufacturing Defect
Lupin Pharmaceuticals is recalling Desloratadine 5mg tablets distributed nationwide because N-Nitroso impurity levels exceeded acceptable limits. Affected lots expire in January 2024.
Product
DESLORATADINE — DESLORATADINE (DESLORATADINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0223-2024·2024-01-17
Tizanidine 4mg Tablets Recalled for Contamination with 2mg Tablets
Dr. Reddy's Laboratories is recalling Tizanidine 4mg tablets due to the presence of 2mg tablets in bottles. About 38,952 bottles were distributed nationwide.
Product
TIZANIDINE — TIZANIDINE (TIZANIDINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0218-2024·2024-01-10
Peritoneal Dialysis Solution Recalled for Lack of Sterility Assurance
Fresenius Medical Care is recalling 69,590 bags of DELFLEX Peritoneal Dialysis Solution due to lack of sterility assurance. The affected lot was distributed nationwide.
Product
DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0215-2024·2024-01-10
OTC Cough Medicine Recalled for Potential Water Contamination Risk
Seaway Pharma Inc. recalled Premier Value Tussin Cough DM due to possible microbial contamination in manufacturing water. No contamination was found in finished products and no illnesses have been reported.
Product
Premier Value Tussin Cough DM, Dextromethorphan HBr...Cough Suppressant, Guaifenesin...Expectorant, Alcohol Free, 8 FL OZ (237 mL) bottle, Distributed by: Pharmacy Value Alliance, LLC, 407 East Lancaster Avenue, Wayne PA 19087, UPC 8-40986-03789-4.
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0213-2024·2024-01-10
Prescription Oral Solution Eprontia Recalled for Out-of-Specification Impurity
Azurity Pharmaceuticals recalls Eprontia (topiramate) oral solution nationwide because routine stability testing found an out-of-specification impurity. The chemical defect raised concerns about the drug's purity and patient safety.
Product
EPRONTIA — EPRONTIA (TOPIRAMATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0216-2024·2024-01-10
OTC Nasal Decongestant Recalled Due to Manufacturing Process Deviation
Quality Choice No Drip nasal decongestant is being recalled due to a manufacturing deviation in water purification. No contamination was detected in the finished products.
Product
OXYMETAZOLINE HYDROCHLORIDE — OXYMETAZOLINE HYDROCHLORIDE (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0214-2024·2024-01-10
Oxymetazoline Nasal Spray Recalled Due to Manufacturing Process Deviation
Seaway Pharma is recalling oxymetazoline nasal spray due to manufacturing process deviations. No contamination was found in the final products.
Product
OXYMETAZOLINE HYDROCHLORIDE — OXYMETAZOLINE HYDROCHLORIDE (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0217-2024·2024-01-10
Nasal Decongestant Recalled for Possible Manufacturing Water Contamination
Quality Choice No Drip Nasal Decongestant is being recalled because purified water used in manufacturing may have contained microbial contamination. No contamination was detected in the final products.
Product
OXYMETAZOLINE HYDROCHLORIDE — OXYMETAZOLINE HYDROCHLORIDE (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-0206-2024·2024-01-03
Supplement Capsules Recalled for Undeclared Sildenafil Content Nationwide
Magnum XXL 9800 capsules contain undeclared sildenafil and were marketed without FDA approval. The product was distributed nationwide via Amazon.
Product
Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759 99300 7. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0207-2024·2024-01-03
Brut Classic Antiperspirant and Deodorant Recalled for Benzene Contamination
Brut Classic Antiperspirant & Deodorant in 4 oz and 6 oz aerosol cans is being recalled due to benzene contamination. The recall affects all lots distributed in the United States and Canada.
Product
Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0209-2024·2024-01-03
Sure Regular Antiperspirant Deodorant Aerosol Recalled for Benzene Contamination
Sure Regular Antiperspirant Deodorant Aerosol (6 oz cans) sold nationwide in the US and Canada is being recalled due to benzene contamination. All lots expiring on or before August 2023 are affected.
Product
Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0208-2024·2024-01-03
Sure Unscented Deodorant Aerosol Recalled for Benzene Contamination
Sure Unscented Deodorant Aerosol is being recalled nationwide due to benzene contamination. Consumers should stop using affected cans and contact the manufacturer.
Product
Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0179-2024·2024-01-03
Enoxaparin Sodium Injection recalled due to improper storage conditions
Sandoz Inc is recalling Enoxaparin Sodium Injection (batch SAH06821A) nationwide due to CGMP deviations: products were exposed to temperatures outside labeled storage conditions, potentially affecting drug stability.
Product
ENOXAPARIN SODIUM — ENOXAPARIN SODIUM (ENOXAPARIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0161-2024·2024-01-03
Respiratory inhalation medication recalled for temperature storage deviation
Cardinal Healthcare is recalling an ipratropium bromide and albuterol sulfate inhalation solution nationwide after the product was exposed to temperatures outside labeled storage conditions. The deviation may affect drug potency.
Product
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE — IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE (IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0204-2024·2024-01-03
FDA Recalls AnazaoHealth Injectable Vitamin Solution Due to Particulate Matter
AnazaoHealth Corporation is recalling 3,363 vials of Thiamine HCl/Pyridoxine HCl injection solution nationwide due to the presence of particulate matter. Affected lots are identified by lot numbers and expiration dates listed by the FDA.
Product
Thiamine HCl/Pyridoxine HCl 20 mg/mL /100mg/ml Injection Solution, 30mL Amber Glass Vial, Rx only, AnazaoHealth, 7465 W. Sunset Road, Las Vegas, NV, NDC 72682-8721-3.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0200-2024·2024-01-03
Warfarin Sodium tablets recalled due to improper storage temperature exposure
Cardinal Healthcare recalls Warfarin Sodium tablets distributed nationwide due to products being exposed to improper storage temperatures.
Product
WARFARIN SODIUM — WARFARIN SODIUM (WARFARIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0181-2024·2024-01-03
Lansoprazole Suspension Recalled Due to Temperature Storage Deviations
A prescription lansoprazole suspension has been recalled because batches were exposed to temperatures outside the manufacturer's labeled storage range. This manufacturing quality issue affects Batch 21025A nationwide.
Product
FIRST LANSOPRAZOLE PT 3MG/ML, 300ML, Rx Only, Distributed By: CutisPharma, Inc., Woburn, MA 01801. NDC: 65628-080-10
Category
Drug
Distribution
Distributed nationwide

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1801–1825 of 5047