Drug Recalls

Philips Respironics Recalls V60 and V60 Plus Ventilators Equipped with High Flow Therapy Software Versions 3.00 and 3.10 Due to Risk of Receiving Reduced Oxygen

Posted on by Editor

Date: 08/03/2021

Product type:  Null

Recalled Product

  • V60 Plus ventilators and all V60 ventilators upgraded to enable High Flow Therapy (software version 3.00 and 3.10)
  • Distribution Dates: May 1, 2009 to June 2, 2021
  • Devices Recalled in the U.S.: 16,535
  • Date Initiated by Firm: June 18, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-v60-and-v60-plus-ventilators-equipped-high-flow-therapy-software