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

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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
12/10/2021	Rompe Pecho	Liquid Cold & Flu symptom relief	Microbial contamination	Efficient Laboratories, Inc
12/07/2021	Teligent Pharma, Inc.	Lidocaine HCl Topical Solution USP 4%, 50ml	Super potent	Teligent Pharma, Inc.
12/07/2021	Edge Pharma, LLC	All drugs compounded at Edge Pharma, LLC	Process issues that could lead to a lack of sterility assurance for products intended to be sterile and could impact the safety and quality of non-sterile products	Edge Pharma, LLC
12/03/2021	Gilead	Veklury® (remdesivir 100 mg for injection)	Presence of glass particulates	Gilead Sciences Inc.
12/02/2021	Sandoz	Enoxaparin Sodium Injection	Exposure to high temperatures may have impacted product effectiveness.	Sandoz, Inc.
11/23/2021	Old Spice, Secret	Old Spice and Secret Aerosol Sprays	Due to the presence of benzene	The Proctor & Gamble Company
11/22/2021	Sagent	Levetiracetam Injection	Lack of sterility assurance	Sagent Pharmaceuticals, Inc.
11/19/2021	American Screening	Hand Sanitizer	Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption	American Screening LLC
11/17/2021	Odor-Eaters®	Oder Eaters spray products	Due to the presence of benzene	Odor-Eaters®, owned by Blistex Inc.
11/15/2021	SterRx, LLC	SterRx products intended to be sterile	Lack of sterility assurance	SterRx, LLC

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