Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ambu¿ VivaSight 2 DLT Endobronchial tube Recalled by Ambu Inc. Due to Ambu has received complaints on Ambu¿ VivaSight 2...
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¿ VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr (Catalog Number 412391000), 41 Fr (Catalog Number 412411000)
Quantity: 1824
Why Was This Recalled?
Ambu has received complaints on Ambu¿ VivaSight 2 DLTs regarding hyper angulation of the distal end. The hyper angulation can lead to an increased risk of complications during intubation and potential airway injury.
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