Ambu® Vivasight™ 2 DLT
Brand(s)
Last updated
Summary
Product
Ambu® Vivasight™ 2 DLT
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Industry
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Ambu® Vivasight™ 2 DLT | 1000891676 1000973466 1000883071 1000895358 1000963431 1000973443 1000983051 1000969604 | 412391000 412351000 412411000 412371000 |
Issue
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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies
| Ambu A/S |
| Baltorpbakken 13, Ballerup, Denmark, 2750 |
Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-76236
Get notified
Receive notifications for new and updated recalls and alerts by category.