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Ambu® vivasight™ 2 dlt
Official notice
2 Oct 2024
Last checked
2 Oct 2024
An official Health Canada notice concerns Ambu® vivasight™ 2 dlt. Issue with the 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. Recall start date: September 24, 2024 Published 2024-10-02.
What to do now
Contact the manufacturer if you require additional information.
Recall number
76236
Official notice
2024-10-02
The hazard
The hazard
Issue with the 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. Recall start date: September 24, 2024
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Turn on recall alertsAffected products
Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Ambu A S, Ambu® Vivasight™ 2 Dlt.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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