Ambu recalls VivaSight 2 DLT endobronchial tubes with hyperangulation risk during intubation. Affected models include 35-41 Fr with specific lot numbers. No remedy provided in recall notice.
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.
Ambu is recalling VivaSight 2 DLT endobronchial tubes that may hyperangle during intubation, potentially causing airway injury. This risk affects specific sizes and production lots.
The tubes may bend excessively at the end during insertion, increasing the chance of airway damage or complications during intubation. This hyperangulation can occur even with normal use.
Healthcare professionals using these tubes during intubation procedures are most at risk. Patients receiving intubation care with affected tubes could experience complications.
Check the tube size (35-41 Fr) and lot numbers listed in the recall notice. The specific lot ranges are provided for each tube size in the product description.
Identify the tube size and lot number to confirm if your item is affected.
Ambu has received complaints about hyperangulation of the distal end, which can lead to complications during intubation and potential airway injury.
The affected models are 35 Fr (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr (Catalog Number 412391000), and 41 Fr (Catalog Number 412411000) with specific lot numbers.
The recall notice does not provide a remedy; affected items should be checked against the listed lot numbers.
We’ve drafted a message you can send Ambu to request your refund or repair — edit it as you like.
Subject: Recall Z-0261-2025 — Ambu Ambu Hello, I own a Ambu that is covered by recall Z-0261-2025 from Ambu. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
