FDAOctober 18, 2023device

Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w

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

The hazard

Their is the potential that software issues may result in flipped image of the virtual Bronchoscope view.

What to do

FDA enforcement status: Ongoing

Brands named

auris healthauris

Recall history

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

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