RecallDepth
Class II Terminated

0.9% Sodium Chloride Injection USP, 50 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira, Inc., Ausitn, TX 78728, NDC 00409-7101-68

Company
Hospira Inc.
Recall Initiated
July 2, 2015
Posted
July 22, 2015
Recall Number
D-1240-2015
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
314600 bags
Firm Location
Lake Forest, IL, United States

Reason for Recall

Lack of assurance of sterility: Potential channel leaks near the threaded vial port.

Distribution

United States

Lot / Code Info

Lot #: 49-084-JT; 49-119-JT

More recalls by Hospira Inc.

View all recalls by this company →

Other recent Class II Drug recalls