Product Safety Recalls

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Remote Diagnostic Technologies Ltd. Recall 92251

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

Remote Diagnostic Technologies Ltd. Recall 92251 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1825-2023
Event ID92251
Event DescriptionPhilips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Product TypeDevices
DistributionUS Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.
Quantity1147
Recall ReasonDefibrillator/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".
Device Classification20230621
Device Code InfoUDI-DI: 07613365002737. Serial numbers prior to 7022.001634
Center Classification Date20230612
Recall Initiation Date20230508
Recalling FirmRemote Diagnostic Technologies Ltd.
Initial Notification Letter
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