Sherpa Nx Active Guide Catheter (2019-04-11)
Sherpa NX Active Guide Catheter Recall Summary The Sherpa NX Active Guide Catheter has been recalled in Canada due to safety concerns with the medical device. This recall affects all units distributed across Canada. The FDA classified this as a Class I recall, indicating a serious potential health risk.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-05-03
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/55007ef2-8a26-4383-8e6e-f0ef03c47c29