FDAFebruary 14, 2020device

The Cogent Hemodynamic Monitoring System. REF58400-000, GTIN 00840619099459; REF 58400-000R, GTIN 0087709094314; REF 58403, GTIN 00840619079505; REF 58401, GTIN 00840619079499 - Product Usage: intended for patients for whom the monitoring of continuous cardiac output and calculated hemodynamic pa...

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

The hazard

Firm identified software issues which leads to the patient ID and patient information not being stored in the system.

What to do

FDA enforcement status: Terminated

Brands named

icu medicalicu

UPCs

0084061909945900877090943140084061907950500840619079499

Recall history

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

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