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 13321–13340 of 17,529 recalls
Recalled Item: Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast-Max Cold & Sinus
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Cold
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine HCl Chewable Tablet
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flurandrenolide Tape
The Issue: Subpotent Drug: Flurandrenolide is subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP
The Issue: Presence of Particulate Matter: The firm produced products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN Sodium Injection USP
The Issue: Presence of Particulate Matter: The firm produced products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium
The Issue: Presence of Particulate Matter: The firm produced products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium
The Issue: Presence of Particulate Matter: The firm produced products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP
The Issue: Chemical Contamination: Product recalled due to an elevated
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP
The Issue: Chemical Contamination: Product recalled due to an elevated
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN Sodium Injection USP 25
The Issue: Presence of Particulate Matter: The firm produced products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium
The Issue: Presence of Particulate Matter: The firm produced products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame oil
The Issue: Incorrect Product Formulation: Vials labeled as Testosterone Cypionate
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ImproVue Ophthalmic Lubricant Drops (1.7% Hypromellose)
The Issue: Failed pH specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONISTAT 1 SIMPLE CURE (Miconazole Nitrate Vaginal Insert) 1200 mg ovule
The Issue: Marketed without an approved NDA/ANDA: The distributed units
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.