Reported Oct 12, 2022 · Ongoing
Philips Respironics DreamWear Full Face Mask
Philips Respironics, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Respironics, Inc. · 1001 Murry Ridge Ln · Murrysville, PA · 15668-8517
Is this the product you have?
- Philips Respironics DreamWear Full Face Mask
- Lot codes and dates
83 of 83 codes
All UnitsModel No.: 11333441133345113337011333711133372113337311333751133376113337711333781133380113338111333821133383113338511333861133387113338811333901133391113339211333931133395113340011334011133405113340611334071133408113341011334111133412113341311334151133416113341711334181133423113342411334251133427113343011334311133432113343311334341133435113343611334381133450113345411352751135276113527711352781135327113538811353891135390
- Amount recalled
- 9,191,280 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Stop using this product now
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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