Brightmatter Guide (2018-10-08)
BrightMatter Guide Recall Summary BrightMatter Guide is a medical device that has been recalled across Canada due to a Class I classification, which indicates a serious safety concern. The specific reason for the recall relates to issues with the device itself, though detailed technical information about the defect is not provided in this notice. This recall affects all BrightMatter Guide devices distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-10-26
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/7fd3ca81-6e04-4a3d-9d05-2241cbdcf732