Philips Respironics recalls DreamWisp Nasal Mask with Over the Nose Cushion due to no known magnetic component risks for patients with implantable devices or metallic eye splinters.
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Philips Respironics is recalling all DreamWisp Nasal Masks with Over the Nose Cushion models because they do not pose a risk of magnetic interference for patients with implantable medical devices or metallic eye splinters. This recall is for safety reassurance, not a hazard.
The recall states there is no contraindication or warning about magnetic components in these CPAP masks. This means the masks do not pose a risk of interfering with implantable medical devices or causing issues for people with metallic eye splinters.
All owners of the DreamWisp Nasal Mask with Over the Nose Cushion are affected. Patients with implantable medical devices or those with metallic eye splinters are most at risk.
Check for model numbers listed in the recall: 1137916, 1137918, 1137921 through 1137955, 1139332 through 1139336, 1144344 through 1144502, 1148409 through 1148917, and other variants ending with RTL, AP, CE, or RC.
Review the model numbers on your mask to see if they match the list provided in the recall.
No, the recall states there is no contraindication regarding magnetic components for patients with implantable devices.
Yes, check model numbers like 1137916, 1137918, 1137921 through 1137955, 1139332 through 1139336, 1144344 through 1144502, 1148409 through 1148917, and other variants ending with RTL, AP, CE, or RC.
The recall does not specify a remedy, so no action is required beyond checking model numbers.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1782-2022 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1782-2022 from Philips Respironics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
