Carto Vizigo 8.5f Bi-directional Guiding Sheath (2021-02-25)
CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath Recall The CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, a medical device used in cardiac procedures, is being recalled across Canada. The specific reason for the recall has not been detailed in the available information. This recall affects all units of this device that were distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2021-03-18
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/befddab3-a4c9-4c83-93f9-663c8738ddb6