RECALL ALERT
Ongoing
XLSX-B7AFC137A5
Actavis: Metformin Hydrochloride Extended-Release Tablets, USP 500mg and 750mg
Recalled by Teva Pharmaceuticals USA Inc.
Classification
—
Reason for Recall
Due to detection of N-Nitrosodimethylamine (NDMA)
Product Details
Product Quantity
Not specified
Product Type
Food
Code Info
Not specified
Voluntary/Mandated
Not specified
Distribution & Geography
Distribution Pattern
Not specified
Company Location
Not specified
Timeline
Report Date
06/05/2020
Recall Initiated
06/05/2020
Classification Date
N/A
Termination Date
N/A
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: September 7, 2026
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