RecallDepth
Class II Terminated

Bacteriostatic Water for Injection, USP, 30 mL vials, Rx only, Mfd. for: Hospira, Inc., Lake Forest, IL 60045 USA. NDC Vial: 0409-3977-01; NDC Carton: 0409-3977-03

Company
Pfizer Inc.
Recall Initiated
September 6, 2019
Posted
September 18, 2019
Recall Number
D-1852-2019
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
185,700 vials
Firm Location
New York, NY, United States

Reason for Recall

Lack of Assurance of Sterility

Distribution

Nationwide US and Puerto Rico

Lot / Code Info

Lot #: W20308, Exp. Dec 1, 2019

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