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Prescription Drugs

💊 Drugs 12,141 recalls

Penicillin Cross Contamination

Mar 3, 2014 Prescription Drugs Nationwide View Details →

Penicillin Cross Contamination

Mar 3, 2014 Prescription Drugs Nationwide View Details →

Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphthalein. Sibutramine and phenolphthalein are not currently marketed in the United States, making this product an unapproved new drug.

Dec 10, 2013 Prescription Drugs Nationwide View Details →

Presence of Foreign Tablets/Capsules: Recall is due to a pharmacist complaint of a "foreign material", identified as Metoprolol Tartrate Tablet USP 50 mg, found co-mingled in a bottle of Ranitidine Tablets USP 150 mg.

Mar 18, 2014 Prescription Drugs Nationwide View Details →

Defective Delivery System: Potential for dose delivery out of specification due to interation of the drug product powder with the lubricant on the interior of the capsule shell.

Mar 27, 2014 Prescription Drugs Nationwide View Details →

Penicillin Cross Contamination

Mar 3, 2014 Prescription Drugs Nationwide View Details →

Presence of Particulate Matter: Potential for small black particles to be present in individual vials, the potential for missing lot number and/or expiry date on the outer carton and the potential for illegible/missing lot number and expiry on individual vials.

Feb 14, 2014 Prescription Drugs Nationwide View Details →

Labeling: Incorrect or Missing Package Insert; The back of the Medication Guide attached to the Package Insert for Ritalin Tablets was printed with information related to Ritalin SR (Sustained Release) Tablets. Both products, Ritalin Tablets and Ritalin SR Tablets utilize a combined Package Insert. The individual Medication Guides are attached to the Package Insert via a perforation. Although t

Mar 3, 2014 Prescription Drugs Nationwide View Details →

Penicillin Cross Contamination

Mar 3, 2014 Prescription Drugs Nationwide View Details →

Penicillin Cross Contamination.

Mar 3, 2014 Prescription Drugs Nationwide View Details →

Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil. Tadalafil and sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.

Apr 30, 2013 Prescription Drugs View Details →

Penicillin Cross Contamination

Mar 3, 2014 Prescription Drugs Nationwide View Details →

Labeling: Incorrect or Missing Package Insert; The back of the Medication Guide attached to the Package Insert for Ritalin Tablets was printed with information related to Ritalin SR (Sustained Release) Tablets. Both products, Ritalin Tablets and Ritalin SR Tablets utilize a combined Package Insert. The individual Medication Guides are attached to the Package Insert via a perforation. Although t

Mar 3, 2014 Prescription Drugs Nationwide View Details →