More recalls have been ordered for a variety of ventilators made by Dutch electronics and technology manufacturer Philips. The company’s troubles started in fall of last year when lines of Philips CPAPs, BiPAPs, and ventilators were recalled over concerns that the sound dampening foam used in the devices could degrade. This degradation could allow particles of the foam to enter the breathing circuits of the machines and ...
FDA Expands Recall of Philips Ventilators
Posted February 9, 2022 in Drug and Medical Device Lawsuits | Product News and Recalls
New Device Could Aid in IVC Filter Removals
Posted January 20, 2022 in IVC Filter Failure | Product News and Recalls
The FDA has cleared Philips to start producing and marketing its CavaClear Laser Sheath IVC filter removal system. The device is the first of its kind and was developed to aid in the removal of IVC filters when other attempts at removing the devices resulted in failure.
The removal, and failed removal, of IVC filters is a long-known issue in the medical community. The ...
continue reading...Philips CPAP Foam Recall Brings Additional Scrutiny to the Company
Posted December 1, 2021 in Drug and Medical Device Lawsuits | Product News and Recalls
Philips has come under increased scrutiny from federal regulators as investigations into the sound-deadening foam it used on various models of its CPAP machines are revealing much deeper problems within the company.
The foam first came to regulators’ attention this past summer after the discovery that it could degrade and enter the breathing circuits of some of the company’s CPAP machines. Initial reports indicated that the foam particles could cause ...
continue reading...Fallout Begins for Philips CPAP Users in Wake of Recall
Posted September 23, 2021 in Drug and Medical Device Lawsuits | Product News and Recalls
Tens of millions of sleep apnea sufferers across the country are being faced with sleepless nights and frustrating days as they try to chart a course of action since learning that their CPAP machines have been recalled. Millions of Philips DreamStation machines were recently recalled by the manufacturer after it was discovered that the foam used in ...
As the delta variant of the COVID-19 pandemic sweeps through largely unvaccinated swaths of populations around the world, certain Philips ventilators and other breathing apparatuses have been pulled from service for a failure to function properly. The severity of the failure has earned the recall a Class I status from the U.S. Food and Drug Administration which is reserved only for the direst of circumstances where continued use of ...
Philips Device Recall Expands with Cancer Risk Warnings
Posted August 24, 2021 in Drug and Medical Device Lawsuits | Product News and Recalls
As electronics manufacturer Philips struggles to cope with its second medical device recall of the year, the news regarding its first recall has just gotten significantly worse. Earlier this year, a variety of Philips ventilators, BiPAP, and CPAP machines were taken out of service and recalled over concerns that the sound-deadening foam used to insulate the machines and make them quieter could enter the breathing circuit and allow ...
