FDAApril 5, 2016drug

Cisatracurium Besylate Injection, 20 mg per 10 mL (2 mg per mL), For intravenous injection, 10 mL Multiple Dose Vial, Rx only, Fresenius Kabi USA, LLC Lake Zurich, IL 60047, NDC 63323-417-10

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Incorrect/ Undeclared Excipient: Firm is recalling product due to an incorrect statement of Preservative free on the individual carton label. The vial label and outer carton label contain the correct statement of 0.9% benzyl alcohol added as a preservative.

What to do

FDA enforcement status: Terminated

Brands named

fresenius kabifresenius

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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