FDAJuly 21, 2023device

Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu visualization devices, portable endoscopy system. Catalog No: 405011000

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

The hazard

Multiple impacts, for example from being dropped, can cause to the Ambu aView 2 Advance to short-circuit and under special circumstances make the lithium-ion battery in the device combust leading to smoke and flames

What to do

FDA enforcement status: Ongoing

Brands named

ambu

UPCs

5707480145089

Recall history

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

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