Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ambu VivaSight 2 DLT Recalled by Ambu Inc. Due to Firm has received complaints on the device concerning...
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 system used for verifying tube placement and repositioning. Catalog numbers 412351000, 412371000, 412391000, 412411000
Quantity: 12,921
Why Was This Recalled?
Firm has received complaints on the device concerning leak/rupture of either the bronchial or tracheal cuff. Leakage during procedure could lead to loss of secure airway and will require re-intubation of patient.
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