On Tuesday, August 3, the U.S. FDA categorized the recent recall of some of Philips’ ventilators as Class 1—the most critical type—stating that their usage could cause injuries or, worse, death. This marks the second Class 1 recall initiated by Philips in 2021.
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Elite Medical Experts shares its take on the voluntary recall of specific Philips Respironics ventilators, BiPAP, and CPAP devices.
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Philips announces a repair and replacement program for specific Philips Bi-Level PAP, CPAP, and mechanical ventilators related to a voluntary recall of the PE-PUR sound abatement foam in these devices.
Read MoreIn the Enforcement Report for the week of January 2, 2013, the FDA listed the Class II recall of the Extended Brilliance workspace (EBW) in order to update the system.
Read MorePhilips announced that it will voluntarily recall approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs), due to the possibility of a memory chip failure that may render the device inoperable.
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