drugs Class II Updated 2013-11-27

Hospira Inc. recalls Ondansetron Injection, USP, 4 mg/2 mL (2 mg/mL), 2 mL Single

Recalled Product

Ondansetron Injection, USP, 4 mg/2 mL (2 mg/mL), 2 mL Single-dose Vial, Rx Only, Sterile, Hospira Inc., Lake Forest IL 60045, USA, NDC 0409-4755-03

Hazard / Issue

Presence of Particular Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 29-484-DK* and 29-510-DK* Exp 05/01/2015 (lot number may be proceeded with an 01)
View official government recall

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