Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due to Multiple impacts, for example from being dropped, can...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ambu Inc. directly.
Affected Products
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
Quantity: 2689 units
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ambu Inc.
Ambu Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report