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 13641–13660 of 17,529 recalls
Recalled Item: Hackensack University Med Ctr (NJ) 5% Dextrose Neonatal Solution
The Issue: Non-Sterility: Out of specification results for the sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: St Lukes East Lees Summit (MO) Protein Bag
The Issue: Non-Sterility: Out of specification results for the sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: J-TAN D PD Drops (bromphenirame maleate 1 mg and pseudoephedrine
The Issue: Labeling: Not Elsewhere Classified: Product is labeled "Dye
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules
The Issue: Failed Capsule/Tablet Specifications: Actavis has received several complaint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules
The Issue: Failed Capsule/Tablet Specifications: Actavis has received several complaint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules
The Issue: Failed Capsule/Tablet Specifications: Actavis has received several complaint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxocobalamin Injection Solution 1 mg/mL Inj.
The Issue: Presence of Particulate Matter; preservative may not have
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glutathione 200 mg/mL Injectable
The Issue: Incorrect Product Formulation: An incorrect gas was used
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 7-MENT ALPHA ADVANCED MASS BUILDER (7a-methyl-estra-4-en-3
The Issue: Marketed without an approved NDA/ANDA - These products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: M14-MENT ADVANCED MASS BUILDER (7a-Methyl-estra-4-en-3
The Issue: Marketed without an approved NDA/ANDA - These products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SWOLL-250 SUPER MASS BUILDER QUAD STACK (18-Methylestr-4-en-3-one-17b-ol 15mg
The Issue: Marketed without an approved NDA/ANDA - These products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALO-70 MEGA MASS BUILDER (4-chloro-17a-methyl-androst-1
The Issue: Marketed without an approved NDA/ANDA - These products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRASTAIN PRO-ANABOLIC MASS AND HARDENING COMPLEX (Estra-4
The Issue: Marketed without an approved NDA/ANDA - These products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: M1-ALPHA LABS MEGA MASS BUILDER (M1A
The Issue: Marketed without an approved NDA/ANDA - These products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROFESSIONAL FORMEXX BLACK (AromaMaXX 250mg: 13-dimethyl-1
The Issue: Marketed without an approved NDA/ANDA - These products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: sulfur8(R) medicated anti-dandruff conditioner
The Issue: Failed pH specification: Product pH test value of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Lotion USP
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP
The Issue: Labeling: Illegible Label: Sandoz Inc. is recalling of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BELVIQ¿ (Lorcaserin HCl) Tablets
The Issue: Labeling:Missing Label: Bottles may not have a product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops A.C. (Tetrahydrozoline HCl 0.05%
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.