Mako Guidance Module (2019-06-11)
Mako Guidance Module Recall The Mako Guidance Module, a medical device used in surgical procedures, is being recalled across Canada. The recall was issued due to issues with the device classified as a Class I medical device concern. This recall affects patients and healthcare facilities that have received or used this device in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-07-05
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/160514b8-ab65-419e-9a7b-42a766912bcc