Lupin Pharmaceuticals Inc.: Glucagon Emergency Kit for Low Blood Sugar,
Recall reason: CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.. Recalled by Lupin Pharmaceuticals Inc.. Distribution: Nationwide within the U.S.. Classification (Class I — serious health hazard). Affected lots/NDC/dates: Kit Lots: WB00010, Exp. Date Jan 2027; WB00017, WB00019, Exp. Date Feb 2027; WB00070, Exp. Date Jun 2027; WB00077, WB000. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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