Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Philips Respironics Amara View Minimal Contact Full-Face Mask Recalled by Philips Respironics, Inc. Due to No contraindication/warning regarding magnetic components in CPAP masks...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Respironics, Inc. directly.
Affected Products
Philips Respironics Amara View Minimal Contact Full-Face Mask
Quantity: 5,661,639 units
Why Was This Recalled?
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Respironics, Inc.
Philips Respironics, Inc. has 85 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report