US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 13, 2014 (12 years ago)

Metformin Hydrochloride Tablets USP 1000 mg, 500 tablets Rx Only, Manufactured by Blu…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective container: Product distributed without inner seal on bottles.

What was recalled

Metformin Hydrochloride Tablets USP 1000 mg, 500 tablets Rx Only, Manufactured by Blu Caribe Dorado PR 00646. Distributed by Blu Pharmaceuticals Franklin NY 42134, NDC 24658-0292-05

Recalling firm
Blu Pharmaceuticals Inc
NDC code
24658-0292-05
Origin
KY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1302-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Chloride recalls

See all