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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