Exalt Model D Single-use Duodenoscope
Recall Summary The Exalt Model D Single-Use Duodenoscope is being recalled in Canada due to revised instructions for use. This medical device is classified as a Class I recall, which is the most serious type. The product was distributed across Canada.
- Product
- Exalt Model D Single-Use Duodenoscope
- Reason
- Revised instructions for use
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-03-14
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b16740b4-e1d4-4cd9-84a3-e8c91989d288