Newsweek

Philips Recall of Select V60 Ventilators Classified by FDA As 'Most Serious Type of Recall'

Philips Respironics, the U.S.-based health care company owned by Dutch technology firm Philips, has recalled a selection of its V60 ventilator devices due to a risk of "receiving reduced oxygen." The ...
Becker's Hospital Review

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. The FDA classified the recall as a class 1, the ...
Medscape

FDA: Urgent Device Correction, Recall for Philips Ventilator

The US Food and Drug Administration (FDA) has announced a Class I recall for Philips Respironics V60 and V60 Plus ventilators, citing a power failure leading to potential oxygen deprivation. Class I ...
USA Today

Philips Respironics Issues Voluntary Recall Notification/Field Safety Notice* for the V60 Ventilator Product Family

Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that its subsidiary Philips Respironics is notifying customers of its V60/V60 Plus and V680 ventilators ...
BioWorld

Philips Respironics adds V60 ventilators to list of recalled devices

Murrysville, Pa.-based Philips Respironics Inc. has had its share of troubles with its devices for respiratory use, including several CPAP machines. The FDA reported March 21 that the company’s V60 ...