Philips Respironics, Inc.: Medical Device Recall in 2023 - (Recall #: Z-2631-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class I

Date Initiated: August 25, 2023

Date Posted: October 4, 2023

Recall Number: Z-2631-2023

Event ID: 93015

Reason for Recall:

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

Status: Ongoing

Product Quantity: 15 (14 US; 1 OUS)

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated