Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Philips Respironics V60/V60 Plus Ventilator Recalled by Philips Respironics, Inc. Due to Power Management PCBAs may malfunction, causing a power...

Date: August 25, 2023
Company: Philips Respironics, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Philips Respironics, Inc. directly.

Affected Products

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

Quantity: 15 (14 US; 1 OUS)

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed to 4 states: CA, OH, OR, SC

Affected (4 states)Not affected

About Philips Respironics, Inc.

Philips Respironics, Inc. has 85 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report