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 ...
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 ...
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 ...
Medical device manufacturer Philips announced the company will expand on a previous recall in an ongoing effort to remove equipment that could have a contaminant in one of the plastic components.
16don MSN
The FDA rarely forces manufacturers to recall dangerous medical devices, watchdog report finds
The post The FDA Rarely Forces Manufacturers to Recall Dangerous Medical Devices, Watchdog Report Finds appeared first on ProPublica.
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 ...
Eight deaths and 13 injuries have been associated with a class I recall of Philips Respironics’ BiPAP ventilators. FDA noted that the devices may unexpectedly reboot or enter an interoperative state.
Sept 8 (Reuters) - Paris prosecutors opened a criminal probe into Philips (PHG.AS), opens new tab in June over its recall of sleep apnea devices, probing possible charges including aggravated fraud ...
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