Fresenius Kabi USA, LLC: 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL
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# 6402153, Exp Date: 11/30/2026; Batch# 6402297, 6402298, Exp Date: 01/31/2027; Batch# 6402377, 6402378, 6402379, E. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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