# FDA recall Z-2025-2023

> **DRE Medical Group Inc** · Class II · device recall initiated 2023-05-15.

## Product

Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Model Number: R1053618 and R1076709.  These are retrofitted device.

## Reason for recall

Devices were imported with Japanese Language and NIST Oxygen Gas Fittings and retrofitted, may pose a serious health risk as the gas pathway of these devices may be contaminated.

## Distribution

US: CA, FL

## Key facts

- **Recall number:** Z-2025-2023
- **Recalling firm:** DRE Medical Group Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-15
- **Report date:** 2023-07-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Louisville, KY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2025-2023

## Citation

> AI Analytics. FDA recall Z-2025-2023. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-2025-2023. Source: US FDA. Licensed CC0.

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