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FDAMay 8, 2023device

Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020

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

The hazard

Defibrillator/pacemaker module (DPM) may encounter a problem causing communication from the Mainboard to the DPM to fail, leading to no or ineffective pacing with displayed error message "HW failure DPM".

What to do

FDA enforcement status: Ongoing

Brands named

remote diagnostic technologiesremoteremote diagnostic

UPCs

07613365002737

Recall history

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

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Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 — Recall Details · AllClear