# FDA recall Z-2631-2023

> **Philips Respironics, Inc.** · Class I · device recall initiated 2023-08-25.

## Product

Philips Respironics V60/V60 Plus Ventilator,     PCBA Part Number: 453561544461    V60 Device Part Numbers 1053617 (US) and 1137276 (Philippines)

## Reason for recall

Power Management PCBAs may malfunction, causing a power failure leading to ventilator loss of function.

## Distribution

US Distribution to states of: OH, CA, SC, OR; and OUS country of: Philippines.

## Key facts

- **Recall number:** Z-2631-2023
- **Recalling firm:** Philips Respironics, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-25
- **Report date:** 2023-10-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Murrysville, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2631-2023

## Citation

> AI Analytics. FDA recall Z-2631-2023. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2631-2023. Source: US FDA. Licensed CC0.

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