Fresenius Kabi USA, LLC: 0.9% Sodium Chloride Injection, USP, (4,500 mg per 500
Recall reason: Lack of Assurance of Sterility. Recalled by Fresenius Kabi USA, LLC. Distribution: US Nationwide , Alaska, and Puerto Rico.. Classification (Class II — potential health risk). Affected lots/NDC/dates: Batch# 24LU10013, 24LU10014, Exp Date: 09/30/2027; Batch# 24NU10001, 24NU10002, Exp Date: 10/31/2027.. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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