Reported Jun 21, 2023 · Ongoing
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Remote Diagnostic Technologies Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Remote Diagnostic Technologies Ltd. · Farnborough Aerospace Centre · Farnborough, N/A · N/A
Is this the product you have?
- Philips Tempus LS-Manual Defibrillator
- Part Number00-3020
- Lot codes and dates
- UDI-DI07613365002737. Serial numbers prior to 7022.001634
- Amount recalled
- 1147
Where it was sold
Why it was 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".
This product could cause temporary or reversible health problems — stop using it.
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