Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Reported: June 21, 2023 Initiated: May 8, 2023 #Z-1825-2023
Product Description
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
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".
Details
- Recalling Firm
- Remote Diagnostic Technologies Ltd.
- Units Affected
- 1147
- Distribution
- US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.
- Location
- Farnborough, N/A
Frequently Asked Questions
What product was recalled? ▼
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020. Recalled by Remote Diagnostic Technologies Ltd.. Units affected: 1147.
Why was this product recalled? ▼
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".
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 21, 2023. Severity: Moderate. Recall number: Z-1825-2023.
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