drugs Class II Updated 2013-09-04

Hospira, Inc. recalls Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospi

Recalled Product

Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01

Hazard / Issue

Lack of Assurance of Sterility: Either a loose crimp or no crimp was applied to the fliptop vials.

Issued by

FDA

Distribution: Naitonwide
Lot/Code Info: Lot 25048DK Exp. 01/15
View official government recall

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