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

5626–5650 of 17772

SevereFDA (Drugs)·D-0165-2021·2020-12-23
Cipla Recalls Azacitidine Injection Vials Due to Sterility Concerns
Cipla is recalling 2,151 vials of Azacitidine for Injection due to potential sterility issues caused by improper sealing.
Product
Azacitidine for Injection 100 mg/vial For Subcutaneous and Intravenous Use Only Single-Dose Vial Manufactured by Shilpa Medicare Limited Jadcherla -509301 INDIA Distributed by: Cipla USA, Inc. 10 Independence Blvd, Suite 300 Warren, NJ 07059 NDC 69097-805-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0141-2021·2020-12-23
Advanced Nutriceuticals Recalls GHK-CU Vials Due to Sterility Concerns
Advanced Nutriceuticals is recalling GHK-CU vials because production processes cannot assure sterility. The product was distributed in seven states.
Product
GHK-CU, 10 MG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
Category
Drug
Distribution
7 states
SevereFDA (Drugs)·D-0140-2021·2020-12-23
FDA Recalls Thymosin Beta-4 Vials Due to Sterility Concerns
Advanced Nutriceuticals, LLC is recalling Thymosin Beta-4 vials because production processes cannot assure sterility. The product was distributed in seven states.
Product
THYMOSIN BETA - 4, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
Category
Drug
Distribution
7 states
SevereFDA (Drugs)·D-0143-2021·2020-12-23
Advanced Nutriceuticals Recalls LL-37 Vials Due to Sterility Concerns
Advanced Nutriceuticals is recalling LL-37 vials because production processes cannot assure sterility. The product was distributed to seven states.
Product
LL-37, 2000 MCG/ML, 2 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
Category
Drug
Distribution
7 states
HighFDA (Drugs)·D-0161-2021·2020-12-23
CitruGel Hand Sanitizer Recalled for Subpotent Drug Content
Simex Logistics SA de CV is voluntarily recalling 1,800 bottles of CitruGel Hand Sanitizer because the product is subpotent.
Product
CitruGel Hand Sanitizer Advanced Formula 70% Alcohol Fresh Lemon Scent, 33.81 FL OZ (1L), Distributed By Citru Gel Inc. Henderson, NV 89052 www.citrugel.com NDC: 78247-002-01
Category
Drug
Distribution
4 states
ModerateFDA (Drugs)·D-0151-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Impurity
Taro Pharmaceuticals is recalling Equate Athlete's Foot cream because an unknown impurity was detected above specification limits.
Product
CLOTRIMAZOLE — CLOTRIMAZOLE (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0157-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling Best Choice Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Best Choice, Clotrimazole Cream, USP 1%, Antifungal, NET WT 0.5 OZ (14.2g), Distributed by: Valu Merchandisers, CO . 5000 Kansas Ave. Kansas City, KS 66106 Made in Canada. UPC 0-70038-20355-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0146-2021·2020-12-23
Zydus Recalls Lansoprazole Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling 22,848 cartons of Lansoprazole 30 mg tablets nationwide because they failed to meet dissolution specifications.
Product
LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0167-2021·2020-12-23
AvKARE Recalls Sildenafil Tablets Due to Packaging Mix-Up with Trazodone
AvKARE Inc. is recalling 38,715 bottles of Sildenafil 100 mg tablets because they were inadvertently packaged with trazodone at a third-party facility.
Product
Sildenafil Tablets USP 100 mg, Rx Only, 100-count Bottle, Manufactured for: AvKARE Pulaski, TN 38478, NDC 42291-748-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0156-2021·2020-12-23
Taro Recalls Rite Aid Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Rite Aid Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
RiteAid Pharmacy RIngworm Cream, Clotrimazole Cream USP, 1%, Antifungal NET W 0.5 oz. (14.2g), Distributed by: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011 Made in Canada. UPC 0 11822 53812 1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0159-2021·2020-12-23
Taro Recalls Clotrimazole Cream Due to Unknown Degradation Impurity
Taro Pharmaceuticals is recalling specific lots of Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Athlete's Foot Cream, Clotrimazole Cream USP, 1%, Antifungal Cream, NET WT 1 oz (30 g), Distributed by: Taro Pharmaceuticals U.S.A. Inc. Hawthorne, NY 10531. Made in Canada. UPC 3 51672 20022 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0148-2021·2020-12-23
Biogen Recalls Vumerity Capsules Due to Dissolution Test Failures
Biogen is recalling 5,307 bottles of Vumerity capsules because they failed dissolution testing. The medication may not release the drug as intended.
Product
VUMERITY — VUMERITY (DIROXIMEL FUMARATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0152-2021·2020-12-23
Taro Recalls HEB Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling HEB Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
HEB — HEB (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0162-2021·2020-12-23
Simex Logistics Recalls Subpotent Health & Hand Gel Hand Sanitizer
Simex Logistics SA de CV is recalling 19,008 bottles of Health & Hand Gel Hand Sanitizer because the product is subpotent.
Product
Health & Hand Gel Hand Sanitizer 70% Alcohol Content, 33.8 FL OZ (1L), Distributed By Blue Ridge Southern Supply, LLC 1130 Ada St. Blue Ridge, GA 30513 Produced By: Simex Logistics S.A. de C.V. Salvatierra No. 101 Fracc. El Puente C.P. 38040 Celaya, Guanajuato, Mexico. smxcontact
Category
Drug
Distribution
4 states
ModerateFDA (Drugs)·D-0163-2021·2020-12-23
UVT World Gel Hand Sanitizer Recalled for Subpotent Drug Content
Simex Logistics SA de CV is voluntarily recalling UVT World Gel Hand Sanitizer because it is a subpotent drug. The product was distributed in California, Georgia, Nevada, and Texas.
Product
UVT World Gel Hand Sanitizer 70% Alcohol Content, 33.9 FL OZ (1LT), Distributed By UVT World Newport Beach, CA 92660 www.uvt.world Produced By: Simex Logistics S.A. de C.V. Salvatierra No. 101 Fraccionamiento El Puente Celaya, Guanajuato, Mexico Barcode: 7 00306 88677 2
Category
Drug
Distribution
4 states
ModerateFDA (Drugs)·D-0158-2021·2020-12-23
Taro Recalls TopCare Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling TopCare Clotrimazole Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
TOPCARE — TOPCARE (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0164-2021·2020-12-23
Simex Recalls Lavar 70 Gel Hand Sanitizer Due to Subpotent Drug
Simex Logistics SA de CV is recalling Lavar 70 Gel Hand Sanitizer because it is a subpotent drug. The product was distributed in California, Georgia, Nevada, and Texas.
Product
Lavar 70 Gel Hand Sanitizer 70% Alcohol Content, 33.8 FL OZ (1L), Distributed By Blue Ridge Southern Supply, LLC. 1130 Aba St. Blue Ridge, GA 30513 Produced By: Simex Logistics S.A. de C.V Salvatierra No. 101 Fraccionamiento El Puente Celaya, Guanajuato, Mexico, Barcode: 7 05333
Category
Drug
Distribution
4 states
ModerateFDA (Drugs)·D-0160-2021·2020-12-23
Simex Recalls Subpotent +Protec Hands Antibacterial Gel Topical Solution
Simex Logistics SA de CV is recalling +Protec Hands Antibacterial Gel because it is subpotent. The product was distributed in California, Georgia, Nevada, and Texas.
Product
+Protec Hands Antibacterial Gel Topical Solution Instant Sanitizer Hands 70% Alcohol Antiseptic, packaged in bottles of a) 33.8 Oz (1000mL) Barcode: GOOD-GEL-04062020L; b) 127.8 oz (3780mL) Barcode 0723707893163, Distributed by: PS Promotional Services LLC Allen Street #406 Dalla
Category
Drug
Distribution
4 states
ModerateFDA (Drugs)·D-0169-2021·2020-12-23
Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures
Hikma Pharmaceuticals is recalling 1.3 million vials of Sodium Chloride Injection USP 0.9% because pH test results were out of specification.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0154-2021·2020-12-23
Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Athlete's Foot Cream because an unknown degradation impurity was detected slightly above the specification limit.
Product
KROGER — KROGER (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0155-2021·2020-12-23
Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Clotrimazole Cream 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
KROGER — KROGER (CLOTRIMAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0153-2021·2020-12-23
Taro Recalls Kaiser Permanente Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling specific lots of Kaiser Permanente Clotrimazole Cream USP 1% because an unknown degradation impurity was detected slightly above the specification limit.
Product
Kaiser Permanente Clotrimazole Cream USP, 1% Antifungal Cream, NET WT 1 oz (28.4 g), Manufactured by Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T1C1 Distributed by Kaiser Foundation Hospitals Livemore, CA 94551-9756. Made in Canada. NDC 0179-8014-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0147-2021·2020-12-23
SCA Pharmaceuticals Recalls Fentanyl Injection Due to Low Potency
SCA Pharmaceuticals is recalling specific lots of Fentanyl injection for IV or IM use because stability testing showed low potency.
Product
Fentanyl, 250 mcg/ 5mL, Injection for IV or IM use, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-0126-2021·2020-12-16
Shilpa Medicare Recalls Docetaxel Injection Due to Manufacturing Deviations
Shilpa Medicare Limited is recalling 2,008 vials of Docetaxel Injection USP due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Docetaxel Injection USP 160 mg/8mL (20 mg/mL), For Intravenous Infusion Only, Rx Only, 8 mL Single Use Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72485-216-08.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0125-2021·2020-12-16
FDA Recalls Imatinib Mesylate Tablets Due to Manufacturing Deviations
Shilpa Medicare Limited is recalling 4,166 bottles of Imatinib Mesylate 400 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
IMATINIB MESYLATE — IMATINIB MESYLATE (IMATINIB MESYLATE)
Category
Drug
Distribution
Distributed nationwide

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5626–5650 of 17772