Philips Tempus LS-Manual Defibrillator — Class II medical device recall Z-1825-2023
Ongoing recall by Remote Diagnostic Technologies Ltd., reported 2023-06-21, distributed nationwide. Defibrillator/pacemaker module (DPM) may encounter a problem causing communication from the Mainboard to the D
| Recall number | Z-1825-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remote Diagnostic Technologies Ltd., Farnborough, N/A, United Kingdom |
| Recall initiated | 2023-05-08 |
| Classified | 2023-06-12 |
| Reported by FDA | 2023-06-21 |
| Distributed | Nationwide (US) |
| Quantity | 1,147 |
| UPC / GTIN / UDI-DI | 07613365002737 |
| Model numbers | 00-3020 |
Product
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".
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1825-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.