Months after recalling millions of respiratory devices due to health concerns, Philips announced that it would start repairing and replacing its DreamStation CPAP devices in the U.S.
Read MoreThe 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."
Read MoreThe FDA Enforcement Report for the week of March 13, 2013, lists the ongoing recall of the Philips digital Diagnost stationary radiographic system.
Read MoreThe 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.
Read MoreThe FDA Enforcement Report for the week of February 27, 2013, lists the ongoing Class II Recall of the Philips HeartStart XL+ defibrillator/monitor.
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