Cypass Micro-stent Model 241 (2018-08-30)
CyPass Micro-Stent Model 241 Recall The CyPass Micro-Stent Model 241, a medical device used in eye surgery, is being recalled across Canada. The recall is classified as Class I, meaning there is a serious potential health risk. The device was distributed nationwide in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-09-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/6f3e6009-1fce-446c-bf74-662a3c093bb9