# FDA recall Z-1825-2023

> **Remote Diagnostic Technologies Ltd.** · Class II · device recall initiated 2023-05-08.

## 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".

## Distribution

US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.

## Key facts

- **Recall number:** Z-1825-2023
- **Recalling firm:** Remote Diagnostic Technologies Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-08
- **Report date:** 2023-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Farnborough, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1825-2023

## Citation

> AI Analytics. FDA recall Z-1825-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1825-2023. Source: US FDA. Licensed CC0.

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