FDAJuly 2, 2015device

0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.

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

The hazard

Procedures for the acceptance and control of in-process product have not been adequately established.

What to do

FDA enforcement status: Terminated

Brands named

mrp llc dba amusamrpmrp llc

Recall history

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

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