Philips Respironics recalls DreamWear Full Face Masks due to no known magnetic risks for patients with implantable devices or metallic splinters in eyes. All units with specific model numbers are affected.
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 DreamWear Full Face Masks because they don't pose a magnetic risk to patients with implantable devices or those with metallic splinters in their eyes. This recall is for safety reasons to ensure users aren't exposed to potential hazards.
The recall states there is no contraindication or warning about magnetic components in these masks for patients with implantable devices or metallic splinters in the eyes. This means the masks do not pose a risk of interfering with medical devices or causing injury from metallic splinters.
People using Philips Respironics DreamWear Full Face Masks with the listed model numbers are affected. Those with implantable medical devices or metallic splinters in their eyes are at slightly higher risk.
Check the model numbers on the mask: 1133344, 1133345, 1133370, 1133371, 1133372, 1133373, 1133375, 1133376, 1133377, 1133378, 1133380, 1133381, 1133382, 1133383, 1133385, 1133386, 1133387, 1133388, 1133390, 1133391, 1133392, 1133393, 1133395, 1133400, 1133401, 1133405, 1133406, 1133407, 1133408, 1133410, 1133411, 1133412, 1133413, 1133415, 1133416, 1133417, 1133418, 1133423, 1133424, 1133425, 1133427, 1133430, 1133431, 1133432, 1133433, 1133434, 1133435, 1133436, 1133438, 1133450, 1133454, 1135275, 1135276, 1135277, 1135278, 1135327, 1135388, 1135389, 1135390, 1137430, 1137431, 1137437, 1137438, 1137439, 1137440, 1140235, 1143130, 1144347, 1146593, 1146594, 1146595, 1146596, 1146597, 1148363, 1133375RTL, 1133376RTL, 1133377RTL, 1133378RTL, 1133430RTL, 1133431RTL, 1133432RTL, 1133433RTL.
Look for the model numbers listed in the recall notice to confirm if your mask is affected.
The recall states there is no contraindication regarding magnetic components for patients with implantable devices, so they do not pose a risk.
Yes, check the model numbers listed in the recall: 1133344, 1133345, 1133370, and other specific numbers provided in the notice.
The recall does not specify a remedy, so no action is required beyond checking the 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-1781-2022 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1781-2022 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.
