Directcheck™ Whole Blood Control
Recall Summary Bionostics Inc is recalling directCHECK™ Whole Blood Control devices across Canada due to a labelling or packaging defect. This is a Class II recall, meaning the product could cause temporary or minor adverse health effects. The defect affects the labelling or packaging rather than the device itself.
- Product
- directCHECK™ Whole Blood Control
- Reason
- Labelling or packaging defect
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-05-14
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4898f087-50c0-4345-bfd4-bdcd1261cb5c