---
title: "Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V... — FDA record Z-2631-2023 | Is It on Recall"
description: "Power Management PCBAs may malfunction, causing a power failure leading to ventilator loss of function."
url: https://isitonrecall.com/recall/fda-device-z-2631-2023-philips-respironics-v60-v60-plus-ventilator-pcba-part-number-453561544461-v60-device-part-numbers-10/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part Numbers 1053617 (US) and ... — FDA record Z-2631-2023

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 Aug 25, 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/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part Numbers 1053617 (US) and 1137276 (Philippines)
- **Reason**: Power Management PCBAs may malfunction, causing a power failure leading to ventilator loss of function.
- **Classification**: Class I
- **Recalling firm**: Philips Respironics, Inc.
- **Quantity**: 15 (14 US; 1 OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2631-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2631-2023%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 | V60 Device Serial # /PCBA Serial # 201019564 SC23120K8 201014394 SC23120NH 201017048 SC2312133 100246411 SC231116C 100246416 SC231117H 100085632 SC2311127 100013579 SC23110EV 100082334 SC2311138 \*\*\*Updated November 6, 2023\*\*\* 100423818 SC2311168 100293267 SC2312154 100006900 SC2311165 100006889 SC23110MF 201010175 SC231104X (Philippines) \*\*\*Updated July 23, 2024\*\*\* 100385387 SC231108T 201029990 SC2311055 |

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

## Distribution

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

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/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)

## Dates in the source

- **Report date**: Oct 4, 2023
- **Recall initiation date**: Aug 25, 2023
- **Center classification date**: Sep 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-2631-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Philips Respironics, Inc. records](https://isitonrecall.com/brand/philips-respironics-inc/)