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FDA (Device enforcement)Recalled 2023-05-08class ii

Remote Diagnostic Technologies Ltd.: Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020

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".

Details from the source

Reason for recall: 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". Distribution: US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA. Quantity: 1147 Lot/code info: UDI-DI: 07613365002737. Serial numbers prior to 7022.001634

UPC codes

07613365002737

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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