483
Intermountain Medical CenterFDA 483 - Intermountain Medical Center - May 12, 2022
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An FDA inspection of Intermountain Medical Center's Transfusion Service in Murray, UT, revealed a critical failure to report a product at fault in causing a transfusion reaction. Specifically, the facility did not notify its blood supplier of positive bacterial contamination in a Red Blood Cell unit that resulted in a patient's transfusion transmitted infection, violating their own standard operating procedures.
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