Class III
Terminated
Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular, Subcutaneous Use, Rx Only, Hospira, Inc., Lake Forest IL USA, NDC 0406-2336-10.
- Company
- Pfizer Inc.
- Recall Initiated
- July 12, 2017
- Posted
- October 11, 2017
- Recall Number
- D-0001-2018
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 32,276 10 mL vials
- Firm Location
- New York, NY, United States
Reason for Recall
CGMP Deviations: Firm failed to control impurity for color change at the API stage.
Distribution
Nationwide
Lot / Code Info
Lot: 51275DD; Exp. 09/01/17
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