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FDADecember 7, 2022device

Philips Garbin Ventilator, Model Number 1058180B

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

The hazard

The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air inlet, which could result in a reduction in delivered therapy volume or pressure and could cause the device to alarm.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

00606959429338

Recall history

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

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