RECALL ALERT
Terminated
XLSX-E5708E5A54
GSMS Inc.: Losartan potassium tablets
Recalled by Teva Pharmaceuticals USA, Inc.
Classification
—
Reason for Recall
Detection of an impurity – N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)
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
06/11/2019
Recall Initiated
06/11/2019
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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