Class II
Terminated
5% Dextrose and 0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7941-09.
- Company
- Hospira Inc.
- Recall Initiated
- October 14, 2014
- Posted
- December 3, 2014
- Recall Number
- D-0282-2015
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 340,272 bags
- Firm Location
- Lake Forest, IL, United States
Reason for Recall
Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.
Distribution
Nationwide, Puerto Rico, and U.S. Virgin Islands.
Lot / Code Info
Lot # 32-104-JT; Exp. 08/15 Lot # 34-136-JT; Exp. 10/15 Lot # 36-092-JT; Exp. 12/15
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