medical Class II Updated 2023-10-04

Ambu Inc. recalls Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended

Recalled Product

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

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: 5707480145089 Version no.: 054 thru 056; 058 thru 059 Product manufactured prior to Oct 29, 2020
View official government recall

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