FDA recall record

RemedyRepack Metformin Hydrochloride Extended Release 750 mg, 30 count blister cards recall — FDA D-0050-2021

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)

Class IIclassification
D-0050-2021official record ID
Nov 4, 2020report date

Recall record at a glance

Official recordD-0050-2021
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRemedyRepack Inc.
Report dateNov 4, 2020
Recall initiation dateOct 11, 2020
Quantity79/30 count blister cards
LocationIndiana, PA, United States

Official product description

Metformin Hydrochloride Extended Release 750 mg, 30 count blister cards, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA NDC 70518-2480-00

Why the product was recalled

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)

Distribution information

Product was distributed to one customer in PA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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