Ambu® Vivasight™ 2 Dlt

Ambu® Vivasight™ 2 DLT Recall Summary Ambu® Vivasight™ 2 DLT intubation tubes are being recalled in Canada due to performance issues. This is a Class I recall, meaning there is a serious potential for harm. The product was distributed across Canada.

Product

Ambu® Vivasight™ 2 DLT

Reason

Performance

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2024-10-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d96f63c8-d2fd-4224-8a84-7e98914de2f6