# FDA recall Z-0557-2025

> **Remote Diagnostic Technologies Ltd.** · Class III · device recall initiated 2024-10-28.

## Product

Tempus LS-Manual Defibrillator  Model 00-3020    The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode

## Reason for recall

Due to incorrect labels applied to devices during servicing.  Labels contain the incorrect product name and CAT number.

## Distribution

U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.

## Key facts

- **Recall number:** Z-0557-2025
- **Recalling firm:** Remote Diagnostic Technologies Ltd.
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-28
- **Report date:** 2024-12-04

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0557-2025

## Citation

> AI Analytics. FDA recall Z-0557-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0557-2025. Source: US FDA. Licensed CC0.

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