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FDANovember 2, 2020device

Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.

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

The hazard

Potential issues with ventilator navigation ring interface and liquid ingress: 1) The navigation ring may become inoperative or operate intermittently; 2) The navigation ring may cause ventilator parameter values to change erratically during setting entries and adjustments.

What to do

FDA enforcement status: Ongoing

Brands named

respironics californiarespironics

Recall history

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

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