Drug Recalls
Here you'll find every drug recall the FDA has issued, including prescription medications, over-the-counter drugs, compounded pharmacy products, and dietary supplements. We've been tracking these since 2006 and our database updates several times a day so you're always looking at current information.
Drugs get recalled for a number of reasons: contamination during manufacturing, incorrect potency or dosage, failed quality testing (like dissolution or stability tests), sterility problems in injectable products, or labeling and packaging errors that could cause someone to take the wrong dose. If you find a product on this list that you use, please follow the instructions provided by the FDA to take the necessary precautions.
Showing 12101–12120 of 17,529 recalls
Recalled Item: Dryses Aluminum Chlorohydrate Antiperspirant Solution
The Issue: cGMP Deviations; product does not comply with cGMP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dryses Aluminum Chlorohydrate Deodorant for Men Roll-on
The Issue: cGMP Deviations; product does not comply with cGMP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repaskin 50 (octocrylene 7%
The Issue: cGMP Deviations; product does not comply with cGMP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Salises Facial Moisturizing Acne Treatment Gel
The Issue: cGMP Deviations; product does not comply with cGMP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repaskin 30 (octacrylene 4%
The Issue: cGMP Deviations; product does not comply with cGMP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repaskin 50 (octocrylene 7%
The Issue: cGMP Deviations; product does not comply with cGMP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donnatal (Phenobarbital
The Issue: Labeling: Not elsewhere classified - Product label incorrectly
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol USP 99.5%
The Issue: Lack of Assurance of Sterility: The firm is
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone USP 99.5%
The Issue: Lack of Assurance of Sterility: The firm is
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets
The Issue: Presence of foreign substance -This recall has been
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stanozolol 200 mg/ml Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone prop. 200 mg/ml Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPA/PGE1/PHENTO (22.5mg/8.33mcg/0.833mg/ml) Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PGE 20mcg/ml Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPA/PGE1/PHENTO (30mg/40mcg/1mg/ml) Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nandrolone 200 mg/ml Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPA/PHENTO (15mg/0.8333mg/ml) Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPA/PGE1/PHENTO (30mg/50mcg/0.5mg/ml)
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPA/PGE1/PHENTO (30mg/10mg/1mg/ml) Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPA/PHENTO (30mg/1mg/ml) Injection
The Issue: Lack of Assurance of Sterility; FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.