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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