Class I · High riskTerminated Initiated Sep 27, 2011 (15 years ago)
metFORMIN ER Tablets, 500 mg, Rx, Packaged and labeled as metFORMIN Immediate Release…
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Labeling: Label Mix up; product labeled did not indicated Extended Release
What was recalled
metFORMIN ER Tablets, 500 mg, Rx, Packaged and labeled as metFORMIN Immediate Release (IR), Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfr: Amneal/Interpharm, Hauppauge, NY NDC 53746-178-01
Recalling firm
Shamrock Medical Solutions Group LLC
NDC code
53746-178-01
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1448-2014
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.
Reason CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper that had previously been…