FDA Device recall Z-1825-2023
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
- FDA Device
- Class II
- ongoing
- Published 2023-06-21
On 2023-06-21 the FDA classified a Class II recall of Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 by Remote Diagnostic Technologies, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1825-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-05-08 |
| Published | 2023-06-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Remote Diagnostic Technologies |
| Distribution | US |
Product
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Reason
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".
Identifiers
| code_info | UDI-DI: 07613365002737. Serial numbers prior to 7022.001634 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1825-2023%22
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