MAJOR RECAL OF CPAP and BiPAP DEVICES FROM PHILIPS RESPIRONICS

Philips Respironics recently issued an voluntary recall of its continuous positive airway pressure (CPAP) and bi-level positive airway pressure (BiPAP) ventilator devices.

• Consult Philips Respironics’ recall notice
• Consult Health Canada’s recall notice

The company states that the noise-cancelling foam in these devices could present a health risk.

 

How do I check if my CPAP or Bi-PAP is being recalled?

1. All of the recalled devices are from Philips Respironics
2. Verify if your device is one of the models being recalled by Philips

To help you determine if your device is being recalled:

1. Locate the serial number on your device
2. Use the online device identification tool from Philips

 

Do I need to continue my treatment?

Because of the serious risks associated with abruptly stopping treatment for some patients, the Association des pneumologues de la province du Québec (APPQ) issued a press release in which it recommends that patients using a CPAP or BiPAP not stop their treatment before talking to their treating physician if:

• they have severe respiratory issues;
• they had serious episodes of drowsiness during the day before starting their treatment;
• they have any significant pulmonary, cardiovascular or neurological comorbidities (presence of two or more disorders or diseases);
• they perform a critical, security-related job ( professional driver, pilot, heavy machinery operator, etc.).

For any questions related to pursuing treatment, patients should contact their treating physician to determine how to deal with this unique situation.

Consult the notice issued by the college of physicians on July 15

 

Do I need to register my device if it is part of the recall?

• I have a CPAP or BiPAP loaned by the CISSS des Laurentides: We have already registered the device that was loaned to you, therefore, you do not need to do it.
• I have a personal CPAP or BiPAP: You need to register it on the Philips Respironics website.