Philips Respironics Recall

Notice Information

08/29/2022

On August 29^th, Philips Respironics issued a notification to patients utilizing certain sleep therapy masks that contain magnetic headgear.  The five impacted masks are:

1. Amara View Minimal Contact Full-Face Mask
2. DreamWear Full Face Mask
3. DreamWisp Nasal Mask with Over the Nose Cushion
4. Wisp Nasal Masks and Wisp Youth Nasal Masks
5. Therapy Mask 3100 NC/SP

This Urgent Medical Device Correction is intended to inform you that Philips Respironics is updating its existing 'Contraindications' and 'Warning' for the masks listed above.

Contraindication Update: Use of the mask is contraindicated for patients and their household members, caregivers, and bed partners that may be in close vicinity to patients using the masks, that have implanted devices that may be affected by magnets.   

You can disregard this notice IF:

• You are no longer using one of the above-mentioned masks.  No action is required.
• You are using one of the above-mentioned masks, and you or someone that may be in close vicinity to your mask DO NOT have metallic devices or objects implanted. No action is required.

If you are using one of the above-mentioned masks, and you or someone that may be in close vicinity to your mask, DO have metallic devices or objects implanted, please note that Philips Respironics is recommending that you discontinue use of your mask immediately.  Please call us at (866) 907-5337 to order a new mask or obtain replacement clips.

If you received one of the masks above, please click here for additional information.

For more information about this notice, please see here.

06/30/2021

Philips Respironics has issued a voluntary recall on specific sleep therapy and mechanical ventilator devices.

Find out if your device has been affected by this recall by watching this video.

As the next step, we encourage you to click the button below to learn more and register your device with the manufacturer. You will need your Device Name and Serial Number to complete registration.

Register Your Device & More Information!

If you received a DreamStation BiPAP autoSV, BiPAP AVAPS or BiPAP S/T machine, please click here for additional information.

For more information about this recall, please read this letter.