Philips falls substantially and structurally short in handling a recall of apnea devices, the Health and Youth Care Inspectorate (IGJ) confirmed on Thursday after reporting by Nieuwsuur. Patients, who are at risk of inhaling or ingesting foam pieces from the devices, should be much better informed about the replacement and repair plan, according to the inspectorate.
The IGJ reports that this will increase the pressure on Philips. A spokesperson explains that there has been contact with the company about the settlement for some time, but that the inspection has now reached the point where it will make these kinds of statements. “We expect from Philips, among other things, a specific timeline within which patients, practitioners and other stakeholders are informed about the planning and progress of the replacement and repair plan.”
Stiff start
Philips says in a response that it takes the criticism to heart. “It is fair to say that we got off to a rocky start with this security alert and that its sheer size means it is a very complex process with still uncertainties. We regret that, and we are working hard to get people out as soon as possible.” provide more security.” The company expects that the arranging of new or repaired devices for affected customers will be 90 percent complete by the end of this year.
In addition to the problem of the foam rubber bits coming off, there can also be a chemical vapor from the device. Nevertheless, people with apnea who use a Philips device to continue breathing properly in their sleep are advised by the IGJ to continue. The data that is currently available do not indicate any harmful effects in the long term, the inspectorate previously stated.
Stiff breathing
People with apnea have difficulty breathing during their sleep. This not only means that they are not rested in the morning, but also that they run an increased risk of cardiovascular disease, high blood pressure and diabetes in the long term.
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