Drug recall D-851-2013

Class II Terminated reported Aug 14, 2013

Product

Ondansetron Injection, USP, 4mg/2mL, (2mg/ml), 2mL single-dose Fliptop Vial, Rx only, Sterile, NDC 0409-4755-03, Hospira, Inc, Lake Forest, IL 60045.

Reason for recall

Presence of Particulate; lot being recalled as a precaution due to the discovery of 2 particles found in a lot which preceded the recalled lot

Lots and codes

Lot 25394DK, exp. 01/2015

Recall details

Recalling firm
Hospira, Inc., Lake Forest, IL
Quantity
340,600 vials
Distribution
Nationwide
Type
Voluntary: Firm initiated
Recall initiated
May 20, 2013
Terminated
October 28, 2014

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