FDAJanuary 5, 2018device

Hemodynamic monitoring system (HMS), comprised of a Patient Interface Module (Part Number 58401-000 and a User Interface Module (Part Number 58403-000). Intended for patients for whom the monitoring of continuous cardiac output is indicated for diagnostic and prognostic evaluation by a clinician ...

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

The hazard

When continuous cardiac output monitoring with a pulmonary artery catheter is placed in the Pause mode, the catheter thermal coil may continue while in pause mode.

What to do

FDA enforcement status: Terminated

Brands named

icu medicalicu

UPCs

008406190794991731100230100840619079505140130140130

Recall history

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

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