FDAMarch 29, 2021device

Provox Life Night HME, Catalogue Number 8262 - Product Usage: single use heat and moisture exchangers for patients breathing through a tracheostoma.

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

The hazard

Provox Life Night HME may be incorrectly inserted sideways or forcefully through the adhesive coupling potentially occluding or blocking the stoma.

What to do

FDA enforcement status: Terminated

Brands named

atos medical abatosatos medical

Recall history

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

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Provox Life Night HME, Catalogue Number 8262 - Product Usage: single use heat and moisture exchangers for patients breathing through a tracheostoma. — Recall Details · AllClear