Treadmill recall expands to 47,000 units over fire risk, CPSC says

A recall affecting about 47,000 Johnson Health Tech America treadmills has expanded to include additional Matrix Retail ...

Urgent treadmill notice: Owners should check this recall list immediately

Customers should inspect their treadmill to confirm whether they have a power cord bracket installed on the unit. If there is ...
Courthouse News Service

CPAP injuries claim remanded to LA

PITTSBURGH — A Pennsylvania federal court remanded a California woman’s negligence complaint over injuries allegedly caused by a recalled Philips CPAP device back to Los Angeles County Superior Court.
thelundreport

The FDA rarely forces manufacturers to recall dangerous medical devices, watchdog report finds

This story was originally published by ProPublica. Sign up for The Big Story newsletter to receive stories like this one in your inbox. The Food and Drug Administration rarely uses its authority to ...
ProPublica

The FDA Rarely Forces Manufacturers to Recall Dangerous Medical Devices, Watchdog Report Finds

ProPublica is a nonprofit newsroom that investigates abuses of power. Sign up to receive our biggest stories as soon as they’re published. The Food and Drug Administration rarely uses its authority to ...
Reuters

Investor association VEB calls for court inquiry into Philips sleep apnea recall

Sept 24 (Reuters) - (This Sept.24 story has been refiled to remove a picture, with no changes to text) Investor group European Investors-VEB on Wednesday applied for a court inquiry into Philips ...
Becker's Hospital Review

4 medical device recalls and corrections

Here are four of the latest recalls and corrections reported to the FDA. Dexcom corrects G7 and One + CGM apps over missed sensor failure alerts: Dexcom is issuing a correction for certain versions of ...
HME News

Philips removes certain DreamStation devices

WASHINGTON – Philips Respironics has removed certain DreamStation devices due to programming errors that can result in failed therapy modes, according to the U.S. Food and Drug Administration. Philips ...
MassDevice

FDA updates on serious Philips CPAP, BiPAP device recall

Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death. It marks the latest recall development for the Respironics ...
Reuters

Philips faces French criminal investigation over sleep apnea recall

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 ...
MD&M East

Medtech in a Minute: Philips' Latest Recall and More

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.