This article originally appeared in ProPublica. ProPublica is a Pulitzer Prize-winning investigative newsroom. Sign up for The Big Story newsletter to receive stories like this one in your inbox. For ...
The U.S. Attorney's Office says an eastern Washington doctor pled guilty to augmenting recalled medical devices to sell them ...
Dr. Eric Edward Haeger, age 57, of Brewster, Wash., has pleaded guilty to adulterating and misbranding CPAP and BiPAP devices with the intent to defraud or mislead, according to the U.S. Attorney's ...
MedPage Today on MSN
FDA rarely forces manufacturers to recall dangerous medical devices, GAO report says
The FDA rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it's ...
(Reuters) - Paris prosecutors opened a criminal probe into Philips in June over its recall of sleep apnea devices, probing possible charges including aggravated fraud and failure to report safety ...
WASHINGTON (AP) — A massive recall of millions of sleep apnea machines has stoked anger and frustration among patients, and U.S. officials are weighing unprecedented legal action to speed a ...
Technology company Philips plans to cut an estimated 5% of its workforce, about 4,000 positions, due to losses caused by the recall of a sleep apnea product as well as supply chain issues, according ...
Murraysville, Pa.-based Philips Respironics has issued a worldwide recall of its Trilogy Ventilators Models 100, 200 and 202 due to a potentially faulty component on the ventilators’ power boards. The ...
The Illinois lawmakers want an electronic format for medical device makers to quickly and transparently report recall ...
This article originally appeared on ProPublica. The Food and Drug Administration rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it’s sometimes ...
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