RecallDepth
Class II Terminated

Zemplar (paricalcitol) Injection, 5 mcg/mL in 2 mL multi-dose vials, 25 vial carton, Rx only, Manufactured by Hospira, Inc. For Abbott Laboratories, North Chicago, IL 60064, USA, NDC 0074-1658-05

Company
Abbott Laboratories
Recall Initiated
May 14, 2012
Posted
June 27, 2012
Recall Number
D-1388-2012
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
121,000 vials
Firm Location
Abbott Park, IL, United States

Reason for Recall

CGMP Deviations: There is potential that Abbott's third party manufacturer, Hospira, may have applied a foreign (incorrect) stopper to vials in a specific lot of Zemplar Injection.

Distribution

Nationwide

Lot / Code Info

Lot #: 11-122-DK, Exp 10/13

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