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Fresenius Kabi USA LLC (FK USA) Recalls
2 recalls on record · March 20, 2013 to August 28, 2013 · Drugs
August 28, 2013DrugsFDA
Fresenius Kabi USA LLC (FK USA) recalls IRINOTECAN HYDROCHLORIDE INJECTION, 40 mg/2 mL (20 mg/mL), 2 mL Single Dose Vial, Rx only, Manufactured for: APP Pharmac
Hazard: Crystallization: Active pharmaceutical ingredient is precipitating in product solution.
March 20, 2013DrugsFDA
Fresenius Kabi USA LLC (FK USA) recalls CALCIUM GLUCONATE INJECTION, USP, 10% (100 mg/mL), 10 mL, Single Dose Vial, Rx only, For Direct Slow IV or IV Additive U
Hazard: Labeling: Missing label