Philips Respironics recalls Therapy Mask 3100 NC/SP models due to potential magnetic components not affecting 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 Therapy Mask 3100 NC/SP models because they contain magnetic components that could theoretically interact with implantable medical devices or metallic eye splinters. This recall does not pose a serious injury risk to most users.
The mask contains magnetic components that could potentially interact with certain medical implants or metallic eye splinters. However, the recall states there is no contraindication or warning regarding these interactions, meaning the risk is minimal and not a serious hazard.
Patients using the Therapy Mask 3100 NC/SP for CPAP therapy may be affected if they have implantable medical devices or metallic eye splinters. Those without these conditions are not at risk.
Check for the model numbers listed: 1144608, 1144610, 1145038 through 1145074, 1145459, 1145460, 1145461, 1145462, 1145463, 1145464, 1145465, 1145466, 1145467, 1145478, 1145916, 1145917. All Therapy Mask 3100 NC/SP units are affected.
Identify your mask's model number from the list provided in the recall notice.
The recall states there is no contraindication, meaning it does not pose a risk to patients with implantable medical devices.
No, the recall does not require stopping use; it is a low-risk situation with no serious injury mechanism.
The recall does not specify a remedy, so no action is needed unless you have concerns about magnetic components.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1784-2022 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1784-2022 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.
