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 11121–11140 of 17,529 recalls
Recalled Item: Sirolimus Tablets
The Issue: Failed impurities/degradation: out of specification result for impurity
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Urea (50% Urea in a Cream Base)
The Issue: Crystallization; complaints received by the manufacturer of crystals
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin OPTH 0.3% SOL
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CEFTRIAXONE for Injection USP
The Issue: CGMP Deviations: Out of specification (OOS) intermediate in
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHLORHEXIDINE GLUCO. 0.12% ORAL RINSE
The Issue: Failed Impurity/Degradation Specifications: Out of specifications for unknown
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: mitoXANTRONE Injection USP (concentrate)
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Extended Release Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Remeven Cream
The Issue: Crystallization; Complaints that cream appears to have crystallized
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM -
The Issue: Subpotent Drug: Out of Specification assay values on
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg) Capsules
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Oral Suspension
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone HCl
The Issue: Failed Impurities/Degradation Specification; 9 month stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Delayed-release Tablets USP
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mycophenolate Mofetil
The Issue: cGMP deviation; manufacturer is Not Registered with the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: M.l.C. Methyl B12
The Issue: Lack of Assurance of Sterility: FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfacetamide Sodium Ophthalmic Solution
The Issue: Lack of Assurance of Sterility; some lots failed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLEPHERINE 0.5%
The Issue: Lack of Assurance of Sterility: FDA inspection identified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.