---
title: "Philips Respironics V60 Ventilator-Intended to mechanically control or assist... — FDA record Z-2025-2023 | Is It on Recall"
description: "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 ma"
url: https://isitonrecall.com/recall/fda-device-z-2025-2023-philips-respironics-v60-ventilator-intended-to-mechanically-control-or-assist-patient-breathing-by-d/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a prede... — FDA record Z-2025-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 15, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: 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.
- **Classification**: Class II
- **Recalling firm**: DRE Medical Group Inc
- **Quantity**: 22 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2025-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2025-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | USI-DI: 00884838009868 Serial Numbers: Serial Number 100043954 100050078 100052760 100052848 100054619 100054626 100055277 100055557 100058549 100058566 100058837 100058995 100060228 100065373 100069520 100070487 100071122 100072691 100078379 100080232 100080844 201003462 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: CA, FL

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)

## Dates in the source

- **Report date**: Jul 5, 2023
- **Recall initiation date**: May 15, 2023
- **Center classification date**: Jun 28, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2025-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [DRE Medical Group Inc records](https://isitonrecall.com/brand/dre-medical-group-inc/)