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 11821–11840 of 17,529 recalls
Recalled Item: Bull's Genital
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zhong Hua Niu Bian
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tiger King
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guaifenesin Grape liquid 100 mg/5 mL
The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan
The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09%
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate
The Issue: Subpotent Drug; confirmed results by FDA analysis after
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate
The Issue: Subpotent Drug; confirmed results by FDA analysis after
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baclofen
The Issue: Sterility Concerns
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin
The Issue: Non-sterility: presence of mold confirmed by outside laboratory
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baclofen 1 mg/ml in 40 ml NS syringe
The Issue: Sterility Concerns
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IT Custom Compound (BC) Baclofen 2000 mcg/ml
The Issue: Sterility Concerns
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg
The Issue: Presence of Foreign Tablets/Capsules: Presence of a comingled
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APEXXX tablets
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jenesis Dietary Supplement Capsules
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oasis Dietary Supplement Capsules
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: La' Trim Plus Dietary Supplement Capsules
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique
The Issue: Microbial Contamination of Non Sterile Products; testing revealed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.