SoClean Recall Issued For CPAP Cleaners Due to Ozone Exposure Risks
A SoClean2 and SoClean3 recall has been announced due to the risks of ozone exposure linked to the CPAP cleaning devices.
Tag Archives: Philips
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Philips DreamStation CPAP Recall Delays Should Result in Strong FDA Enforcement Action, Including Potential Criminal Charges: Lawmaker
A Senator's letter to the heads of the FDA and the Justice Department calls for swift, aggressive, and potentially criminal, enforcement actions over delays in the Philips DreamStation CPAP recall.
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Philips CPAP Machine Settlement for Class Action Claims Gain Preliminary Approval, As Personal Injury Lawsuit Negotiations Continue
A federal judge has granted preliminary approval for a $479 million Philips CPAP machine class action lawsuit, while hoping a similar agreement can lead to the resolution of tens of…
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FDA Calls Testing By Manufacturer Inadequate in Philips CPAP Recall Update
The FDA has issued an update of the Philips CPAP recall, criticizing the manufacturer for inadequate testing and other ways it has handled pulling the sleep apnea breathing machines from…
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Problems with Philips CPAP Machines Reported 11 Years Before Recall Issued By Manufacturer
A ProPublica report reveals that Philips officials hid thousands of reports of problems with sound abatement foam used in millions of CPAP machines, failing to recall the devices for more…
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MDL Judge Urged to Defer Motions Seeking to Return Philips CPAP Lawsuits To State Courts
Philips is asking a federal judge to delay considering motions to remove some CPAP recall lawsuits to state court until the parties get a better idea of how many plaintiffs…
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Philips CPAP Class Action Settlement Results in Agreement To Pay $479M To Owners of Recalled Machines
A $479 million Philips CPAP class action settlement agreement will resolve claims of economic loss filed by users of the recalled devices.
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Hamilton Ventilator Recall Issued Over Risk of Sudden Failures Due to Software Defect
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Draeger Ventilator Recall Issued Over Toxic Cancer-Causing Foam Particles
The FDA has classified a Carina ventilator PE-PUR foam warning as a class I recall, indicating the breathing devices could put children in particular at an increased risk of cancer…
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Philips Trilogy Evo Ventilator Recall Issued Over Air, Dust Contamination Risks
The FDA warns that 73,000 recalled Trilogy Evo ventilators manufactured by Philips Respironics may be prone to airway blockage from dust and dirt, which has led to at least one…
