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 17461–17480 of 17,529 recalls
Recalled Item: Carbon Dioxide
The Issue: Impurities/Degradation Products: Out Of Specification levels of nitrogen
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ciprofloxacin Tablets
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection
The Issue: Superpotent (Single Ingredient) Drug: Above specification assay results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meloxicam Tablets
The Issue: Tablet Thickness: Recall was initiated due to the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefloquine HCL Tablets
The Issue: Tablet Thickness: Product is being recalled due to
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL)
The Issue: Failed USP Dissolution Test Requirements: Possible out-of-specification dissolut
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL)
The Issue: Failed USP Dissolution Test Requirements: Possible out-of-specification dissolut
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (Methylphenidate) Transdermal System Patch
The Issue: Miscalibrated/Defective Delivery System; exceeded the specification for both
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermaZinc Spray
The Issue: Subpotent (Single Ingredient Drug): The firm is recalling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Balnetar Therapeutic Tar Bath
The Issue: Subpotent (Single Ingredient Drug): out-of-specification result for coal
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Tablets
The Issue: Presence of Foreign Substance(s): A product complaint was
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blue Male Enhancement Pill
The Issue: Marketed without an Approved NDA/ANDA; product found to
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Northstar Zolpidem Tartrate Tablets USP 10 mg. Manufactured for Northstar RX
The Issue: Adulterated Presence of Foreign Tablets: This product is
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Tablets
The Issue: Labeling Illegible: Missing Label; The voluntary recall of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nisoldipine Extended Release Tablets
The Issue: Failed USP Dissolution Test Requirements: Out of Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab.075 mg.
The Issue: Subpotent (Single Ingredient Drug): Low assay at the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets
The Issue: Subpotent (Single Ingredient Drug): Low assay at the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Ten Days Capsule
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Japan Weight Loss Blue Capsules
The Issue: Marketed Without an Approved ANDA/NDA: presence of sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.