INDIANA – Philips Respironics, Inc. is recalling their V60 Ventilators and V60 Plus Ventilators. The ventilators contain Power Management Printed Circuit Board Assemblies (PM PCBA) that were distributed by a third-party warehouse. The PM PCBAs do not meet ventilators standards. Please be aware, this recall is a voluntary correction, not a product removal.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Please be aware, this recall is a voluntary correction, not a product removal.
