Philips Respironics recalls Amara View Minimal Contact Full-Face CPAP masks due to no known magnetic risks for patients with implantable devices or metallic splinters in eyes. No action required.
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Philips Respironics is recalling its Amara View Minimal Contact Full-Face CPAP masks because there's no risk of magnetic components causing harm to patients with implantable devices or metallic eye splinters. This recall does not require any action from users.
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 to these specific groups.
Users of Philips Respironics Amara View Minimal Contact Full-Face CPAP masks. Patients with implantable devices or metallic eye splinters are not at risk from this specific recall.
Check for model numbers 1090602 through 1136626RTL on the mask packaging or label. All units of this product are affected by the recall.
The recall does not require any action from users as there is no risk to patients with implantable devices or metallic eye splinters.
No, the recall states there is no risk to patients with implantable devices or metallic eye splinters, so no action is needed.
Model numbers 1090602 through 1136626RTL are affected.
The recall states there is no contraindication or warning regarding magnetic components for patients with implantable devices or metallic eye splinters, so no risk is identified.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1780-2022 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1780-2022 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.
