Drug Recalls

Philips Respironics Recalls Certain Ventilators and BiPAP Machines Due to Potential Health Risks from PE-PUR Sound Abatement Foam

Posted on by Editor

Date: 07/22/2021

Product type: Medical Device

Recalled Product

  • Mechanical ventilation devices: Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent 200, BiPAP V30, BiPAP A30/Hybrid/A40
  • Serial Numbers: Devices manufactured before April 26, 2021, all serial numbers
  • Distribution Dates: November 5, 2005 to April 23, 2021
  • Devices Recalled in the U.S.: 204,776
  • Date Initiated by Firm: June 14, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-ventilators-and-bipap-machines-due-potential-health-risks-pe-pur