Lupin Pharmaceuticals Inc.: Liraglutide Injection, 18 mg/3 mL (6 mg/mL)
Recall reason: Presence of particulate matter: a white thread-like structure in the cartridge. Recalled by Lupin Pharmaceuticals Inc.. Distribution: Nationwide within U.S. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lots: a) WB00097, WB00094, WB00088, Expires: Jul. 2027; WB00103, Expires: Oct. 2027; WC00016, Expires: Dec. 2027; b) WB0. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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