FDAApril 15, 2025device

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007

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

The hazard

Patient Monitor software update to address issues:1)May freeze at startup with MPM Application error and Attention Restart Required messages,2)Monitor may freeze and reboot at start of 12-lead ECG or after, 3)May reboot after intermittent connection with Smart Mount, 4) 12-lead ECG measurements with Louvain algorithm and software before vx.36 could produce inaccurate rhythm/morphology statements.

What to do

FDA enforcement status: Ongoing

Brands named

remote diagnostic technologiesremoteremote diagnostic

UPCs

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Recall history

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

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