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 6221–6240 of 17,529 recalls
Recalled Item: Colostat
The Issue: Labeling mix-up - Indications on product label are
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYORISAN (isotretinoin capsules
The Issue: Unit Dose Mispackaging: Customer complaint that a carton
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam
The Issue: Defective delivery system; product is not foaming or
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation)
The Issue: Defective delivery system; product is not foaming or
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Yeast Arrest
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AVKARE Ranitidine Tablets
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Oral Solution
The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Silver Bullet
The Issue: Undeclared Active
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 1000 mcg/20 mL (50 mcg/mL) 20 mL in 20 mL Syringe Preservative Free
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 250 mcg/5 mL (50 mcg/mL)
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2500 mcg/250 mL (10 mcg/mL) in 0.9% Sodium Chloride
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2000 mcg/100 mL (20 mcg/mL) in 0.9% Sodium Chloride
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2750 mcg/55 mL (50 mcg/mL) 55 mL Syringe
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2500 mcg/50 mL (50 mcg/mL) 50 mL bag
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 1250 mcg/250 mL (5 mcg/mL) in 0.9% Sodium Chloride
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 800 mcg/200 mL (4 mcg/mL) BUPivacaine HCl 0.1667% 333.4
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluphenazine Decanoate Injection USP 125mg/5mL
The Issue: Discoloration; Hazy solution found in one vial instead
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.