US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 19, 2020 (6 years ago)

Metformin Hydrochloride Extended-Release Tablets USP, 500 mg 1000 Tablets Rx Only…

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

Why it was recalled

CGMP Deviations

What was recalled

Metformin Hydrochloride Extended-Release Tablets USP, 500 mg 1000 Tablets Rx Only Manufactured by: Beximco Pharmaceuticals, LTD. 126, Kathaldia, Tongi, Gazipur, 1711, Bangladesh NDC 76385-128-10

Recalling firm
Bayshore Pharmaceuticals
NDC code
76385-128-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1543-2020

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.

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