drugs Class II Updated 2013-08-28

Fresenius Kabi USA LLC (FK USA) recalls IRINOTECAN HYDROCHLORIDE INJECTION, 40 mg/2 mL (20 mg/mL), 2

Recalled Product

IRINOTECAN HYDROCHLORIDE INJECTION, 40 mg/2 mL (20 mg/mL), 2 mL Single Dose Vial, Rx only, Manufactured for: APP Pharmaceuticals, LLC, Schaumburg, IL 60173, NDC 63323-193-02, UPC 3 63323 19302 7.

Hazard / Issue

Crystallization: Active pharmaceutical ingredient is precipitating in product solution.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 872CZ00101, Exp 12/13
View official government recall

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