RecallDepth
Class II Terminated

Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24

Company
Pfizer Inc.
Recall Initiated
September 1, 2017
Posted
October 4, 2017
Recall Number
D-1177-2017
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
18,725 vials
Firm Location
New York, NY, United States

Reason for Recall

Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.

Distribution

Nationwide in the USA

Lot / Code Info

Lot: 63-075-DK Exp. FEB 2019

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