Febridx (2020-12-21)
FebriDx is a medical device that has been recalled across Canada due to COVID-related issues. The device is classified as a Class I recall, which is the most serious type. The recall affects all FebriDx products distributed in Canada.
- Reason
- COVID - Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-12-31
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ce50b0c5-6723-47a1-9ef6-1c47803e3177