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• #Philips respironics recall full

They were each horrified to hear that the devices they relied on to keep them healthy were actually blowing toxic chemicals into their bodies. The plaintiffs, John Morel and Korinn Gray, were diagnosed with sleep apnea and purchased Philips CPAP machines.

All of these models were manufactured with a polyester-based polyurethane sound abatement foam, exposure to which can cause cancer, respiratory damage, asthma, nausea, vomiting, headache, and possibly other harm. On June 14, 2021, Philips Respironics issued a recall notice in the US for 17 models of its respiratory devices, and Health Canada recalled an additional 35 models in Canada. Thomson Rogers, Rice Harbut Elliott LLP, and Sotos LLP are working together on a national class action on behalf of all persons in Canada who used a Philips CPAP machine, BiPAP machine, or mechanical ventilator which are currently subject to a recall by the company (please see below for a complete list of the affected devices). If you have not already signed up for this class action and would like to receive future updates, please complete the brief questionnaire below. Unfortunately, lawsuits take time, and it is not likely that any resolution will be achieved in the near future.

#Philips respironics recall full

However, this is happening relatively slowly: Philips has advised that this process will take roughly 12 months.įor full details, see their press statement here. Philips has advised that it will repair or replace affected units in Canada and other jurisdictions but has not yet provided a firm timeline to do so.įor customers in the United States, Philips has begun either removing the toxic PE-PUR foam or replacing older models with their DreamStation 2. On September 1, Philips announced its plans to repair or replace the recalled devices. We are aware of these concerns and will factor them into our approach in the lawsuit. We understand that this is a difficult decision. This decision should be based on what is appropriate in your individual circumstance, including any medical advice received. We understand that each individual must make his or her own decision about whether to replace the unit with another model, wait for Philips to repair or replace the model, or continue using their existing model. If you are using the device for medical reasons, you should first consult your physician and follow their advice. Since we launched this action, we have been contacted by many people who have asked for our advice on what to do. Any person in Canada who used one of the recalled Philips machines is automatically a class member.

We anticipate there are over 100,000 Canadians who use or have used a Philips CPAP or BIPAP machine.

We are seeking a full refund or replacement unit for all class members in addition we are seeking damages for pain and suffering caused by adverse health issues, injuries caused by the direct use of these machines as well as damages for the health care costs incurred as a result. This CPAP action seeks to represent class members who purchased and used one of the recalled Philips CPAP or BIPAP machines. Philips CPAP And Respiratory Device Class Action