Ambu Vivasight 2 Dlt Kit
Ambu Vivasight 2 DLT Kit Recall The Ambu Vivasight 2 DLT Kit is being recalled across Canada due to a performance issue. This product is a medical device used in healthcare settings. The recall is classified as Class I, indicating a serious potential health risk.
- Product
- Ambu Vivasight 2 Dlt Kit
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-06-20
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/cadfcdc7-434f-498c-927b-175199330072