FDAJuly 2, 2015drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

hospira

UPCs

00409710168

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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