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The recall extends to 32 devices of the Model 3028 IPG. Inspire Medical Systems is recalling Inspire IV Implantable Pulse Generator (IPG) Model 3028 due to a manufacturing defect.
In June 2021, the FDA first announced the recall of Philips Respironics BiPAP and CPAP devices—which are worn overnight while someone sleeps—as well as ventilators, saying the polyester-based ...
A 2021 recall of Philips breathing devices is related to 561 deaths, the U.S. Food and Drug Administration said Wednesday. 561 deaths linked to recalled Philips sleep apnea machines, FDA says Skip ...
Matthew Stone, 61, was using a Philips CPAP machine for sleep apnea, but fell back on an older device from another manufacturer due to the recall. (Allen J. Schaben / Los Angeles Times)
The company responsible for a global recall of sleep apnea machines will be barred from resuming production at U.S. facilities until it meets a number of safety requirements, under a long-awaited ...
The California-based medical device maker started the recall process on Nov. 20 and has recalled over 20 mill US FDA identifies recall of ResMed's respiratory devices as most serious Skip to main ...
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Jun. 15—Medical equipment company Philips has issued a recall on some products to address possible health risks associated with a foam component meant to help reduce noise. ... (CPAP), and ...
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