The FDA classified the recall as a class 1, the most serious type. There have been four reports of injuries as of April 14.
Philips Respironics recalls all V60 ventilators over power issues
Philips Respironics recalled all V60 and V60 Plus Ventilators on June 3 over a power issue that may cause the devices to shut down without an alarm.
From Foundation to Frontier: Radiology Leaders Discuss Scaling AI in Imaging
Recommended Live Webinar on Jan 29, 2026 11:00 AM - 12:00 PM CST