Product Detail

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

Recall Number D-926-2013

Classification Class II

Code Info Lot 25048DK Exp. 01/15

Product Distributed Qty 345,800 vials

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

Event Detail

Event Id 66050

Product Type Drugs

Status Ongoing

Recalling Firm

Hospira, Inc.
City Lake Forest
State IL
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-08-12

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Naitonwide