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Remote Diagnostic Technologies Ltd. recalls Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Recalled June 21, 2023 · FDA recall Z-1825-2023 · Remote Diagnostic Technologies
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". · FDA Class II
Units
1147
Sold at
US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.
Description
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".
Product
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Manufacturer(s)
Remote Diagnostic Technologies Ltd.
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →