MRP, LLC dba AMUSA 0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only recall — FDA Z-2476-2015
Procedures for the acceptance and control of in-process product have not been adequately established.
Overview of recall records associated with MRP, LLC dba AMUSA, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Procedures for the acceptance and control of in-process product have not been adequately established.
This page summarizes recall records in which the official source identifies MRP, LLC dba AMUSA as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.