Philips Respironics recalls Wisp and Wisp Youth Nasal Masks due to no known magnetic risks for patients with implantable devices or metallic splinters in eyes. All units 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 Wisp and Wisp Youth Nasal Masks because they do not pose a magnetic risk to patients with implantable devices or those with metallic splinters in the eyes. This recall is for safety assurance in medical use.
The recall addresses a lack of warning about magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes. However, the masks do not pose a risk to these users as the hazard is not present in normal use.
Patients using CPAP masks with implantable devices or metallic splinters in the eyes may be affected. Most users are not at risk as the masks do not contain magnetic components that could cause harm.
Check for model numbers 1094050 through 1148366 on the mask packaging. All units of the Wisp and Wisp Youth Nasal Masks are included in this recall.
Look for model numbers on the mask packaging: 1094050, 1094051, 1094053, 1094060, 1094061, 1094062, 1094070, 1094071, 1094072, 1094073, 1109298, 1113954, 1117119, 1118060, 1118061, 1118062, 1118063, 1118064, 1118065, 1118066, 1118067, 1120434, 1137360, 1137361, 1137366, 1137367, 1137368, 1137369, 1137370, 1138989, 1138991, 1138992, 1138993, 1138994, 1138995, 1138996, 1139009, 1148366, or 1094051RTL.
No, the recall states there is no contraindication or warning regarding magnetic components for patients with implantable devices.
Yes, check model numbers on the mask packaging: 1094050 through 1148366, including 1094051RTL.
The recall does not specify a return or 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-1783-2022 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1783-2022 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.
