Search Results for: philips recall

The manufacturer’s recall of approximately 19,200 Philips Respironics V60 ventilators has been given the Class I designation by FDA, indicating "reasonable probability … [of] serious adverse health consequences."

The FDA Enforcement Report for the week of March 13, 2013, lists the ongoing recall of the Philips digital Diagnost stationary radiographic system.

The Enforcement Report for the week of March 6, 2013, lists the ongoing recall of the Mx8000 IDT whole body computed tomography x-ray system distributed by Philips Medical Systems, Highland Heights, Ohio.

The FDA Enforcement Report for the week of February 27, 2013, lists the ongoing Class II Recall of the Philips HeartStart XL+ defibrillator/monitor.

In the Enforcement Report for the week of January 23 the FDA lists the voluntary Class II Recall by Philips Medical Systems (Cleveland) Inc of the computed tomography x-ray system Brilliance workspace portal.