HomeDrug recalls
Medium severity

0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 65219-470-05, Unit of Sale NDC Number: 65219-470-30.

SourceFDA Drug Enforcement
CategoryDrug
SeverityMedium
Statusongoing
Recall dateMarch 11, 2026
ReportedApril 15, 2026
Recalling firmFresenius Kabi USA, LLC
Country / regionUnited States IL

Hazard

Lack of Assurance of Sterility

Affected products

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