A drug recall is the most effective way to protect the public from a defective or potentially harmful product. A recall is a voluntary action taken by a company at any time to remove a defective drug product from the market.

The list below includes voluntary recalls in which public notification has been issued.

See FDA’s role in drug recalls for more information.
See Recalls, Market Withdrawals, & Safety Alerts for all FDA-regulated products.
For recall notices older than 60 days, see recall and safety alerts archive.

Resources for You

• Recalls, Market Withdrawals, & Safety Alerts
• MedWatch: The FDA Safety Information and Adverse Event Reporting Program
• Enforcement Reports
• Drug Safety Communications
• Drug Alerts and Statements
• FDA Recall Information on Twitter
• Basic Reset and Biogenyx Recalled Products

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Terminated Recall - Any -YesNo

A Terminated Recall is a recall where the FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard. Recalls that are not indicated as being terminated are either ongoing or completed.

Date	Brand Name(s)	Product Description	Recall Reason Description	Company Name	Terminated Recall	Excerpt
07/31/2023	Lupin Pharmaceuticals, Inc.	Tydemy oral contraceptive	Out of Specification Results	Lupin Pharmaceuticals, Inc.
07/07/2023	Cipla	Albuterol Sulfate Inhalation Aerosol, 90 mcg (200 Metered Inhalation)	Failure to deliver the recommended dose	Cipla
06/14/2023	Major Pharmaceuticals	Dronabinol Capsules 2.5mg and Ziprasidone Hydrochloride Capsules 20mg	Packaging may contain incorrect product due to labeling mix-up	The Harvard Drug Group, LLC d/b/a Major Pharmaceutical and Rugby Laboratories
05/19/2023	G-SUPRESS DX	Cough Suppressant, expectorant, nasal decongestant pediatric drops	Packaging may contain incorrect product	NOVIS PR LLC
05/19/2023	G-SUPRESS DX	Cough Suppressant, expectorant, nasal decongestant pediatric drops	Device & Drug Safety/Mislabeling	NOVIS PR LLC
05/04/2023	Numerous Brands	Various human and animal drug products	As a result of a bankruptcy, the firm is removing several products from the market due to the discontinuation of the Quality program which would result in the company’s inability to assure that products meet the identity, strength, quality, and purity cha	Akorn Operating Company LLC
05/04/2023	Advil	Over-The-Counter Drugs	Product was stored outside of labeled temperature requirements.	Family Dollar
04/28/2023	Mayne Pharma Inc.	FENTANYL Buccal Tablets CII	Safety updates were omitted in the Product Insert/Medication Guide (MG)	Teva Pharmaceuticals USA
04/26/2023	Pro Power Knight Plus, NUX, Dynamite Super	Male enhancement capsules	Product contains undeclared tadalafil and sildenafil	Gadget Island, Inc.
03/31/2023	Camber	Atovaquone Oral Suspension	Potential Bacillus cereus Contamination	Camber Pharmaceuticals, Inc.

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