Skip to content
Recall Observatory FDA recall evidence

Drug product

Gemcitabine for Injection, USP, 200 mg*/vial, Lyophilized powder in a Single-Use Vial, Rx only, labeled as a) Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-464-20, UPC 3 67457 46420 6; and b) Distributed by Pfizer Labs, Division of Pfizer Inc, New York, NY 10017, Made in India, NDC 0069-3857-10, UPC 3 00693 85710 4.

D-1332-2015

March 23, 2015

Class I

Product summary

Firm
Mylan Institutional LLC
Event
Event 71004
Status
Terminated
Classification
Class I
Quantity
a) 35,197 vials; b) 21,302 vials
Official record key
drug-enforcement:D-1332-2015

Official wording

Reason: Presence of Particulate Matter

Code information: Lot #: a) 7801396, 7801398, 7801401, 7801406, Exp 08/16; 7801427, Exp 09/16; b) 7801089, 7801084, Exp 07/15; 7801110, Exp 08/15

Distribution pattern: Nationwide and Puerto Rico

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    Particulate Matter