Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

1,463 recalls · Class I, newest first

Class I · High risk

Tydemy

Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and MTHFRC-7impurity test

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-904-71 D-1081-2023
Class I · High risk

ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg

Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.

Terminated Labeling / mix-up The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories NDC 0904-6269-08 D-0893-2023
Class I · High risk

G-Supress DX

Product mix-up: incorrect product was found inside the G-Supress DX product carton.

Terminated Labeling / mix-up Novis PR, LLC dba Kramer Novis NDC 52083-655-01 D-0868-2023
Class I · High risk

PrimeZEN Black 6000 capsule

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Volt Candy Wholesale Club D-0453-2023
Class I · High risk

Easy Care First Aid 10 Person 2009 ANSI

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0253-2023
Class I · High risk

CVS First Aid Home

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0252-2023
Class I · High risk

Easy Care First Aid 25 Person 2009 ANSI

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0251-2023
Class I · High risk

Easy Care First Aid 10 Person 2009 ANSI

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0249-2023
Class I · High risk

Easy Care First Aid 25 Person 2009 ANSI

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0248-2023
Class I · High risk

Adventure First Aid 1.5

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0247-2023
Class I · High risk

Adventure First Aid 1.0

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0246-2023
Class I · High risk

Adventure Marine 150

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0245-2023
Class I · High risk

Easy Care first aid Burn Cream

Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.

Terminated Microbial contamination GFA Production Xiamen Co. Ltd. D-0244-2023
Class I · High risk

Epinephrine

Discoloration: Product complaints of the repackaged Epinephrine API being discolored which could result in less effective product

Terminated Failed specification Spectrum Laboratory Products, Inc. D-0180-2023
Class I · High risk

Epinephrine

Discoloration: Product complaints of the repackaged Epinephrine API being discolored which could result in less effective product

Terminated Failed specification Spectrum Laboratory Products, Inc. D-0179-2023
Class I · High risk

Advil Liqui Gels

Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back

Terminated Labeling / mix-up Glaxosmithkline Consumer Healthcare Holdings DBA Haleon D-0183-2023
Class I · High risk

Advil Liqui Gels

Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back

Terminated Labeling / mix-up Glaxosmithkline Consumer Healthcare Holdings DBA Haleon D-0182-2023
Class I · High risk

Advil (ibuprofen)

Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back

Terminated Labeling / mix-up Glaxosmithkline Consumer Healthcare Holdings DBA Haleon D-0181-2023
Class I · High risk

Iohexol (300 mg Iodine/mL)

Labeling: Label Error on Declared Strength: syringes mislabeled as 300 mg iodine/mL contained product 350 mg iodine/mL

Terminated Labeling / mix-up BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy D-0086-2023
Class I · High risk

8.4% Sodium Bicarbonate Injection

Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.

Terminated Packaging defect Exela Pharma Sciences LLC NDC 72572-740-20 D-0080-2023

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