FDASeptember 6, 2022device

Therapy Mask 3100 NC/SP

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Therapy Mask 3100 NC/SP — Recall Details · AllClear