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Teva Pharmaceuticals USA: LOSARTAN POTASSIUM TABLETS, USP 25 mg, Bulk

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.. Recalled by Teva Pharmaceuticals USA. Distribution: Bulk product was distributed to one re-packager in California.. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lots 1207344A, exp. date 06/2020; 1207343A, 1207342A, exp. date 07/2020. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.

Reward FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who purchased the recalled drug or medication. Return it to the pharmacy where you bought it for a full refund. You generally do not need the original receipt — the pharmacist can look up your purchase history.
Source Official Source ↗
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