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

Recalled September 4, 2013 · FDA recall D-926-2013 · Hospira

Hazard

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

Units

345,800 vials

Sold at

Naitonwide

Description

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

Product

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

Manufacturer(s)

Hospira, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →