Tiloop Mesh (2020-04-10)
TiLoop Mesh Recall Summary TiLoop Mesh, a medical device distributed across Canada, has been recalled due to safety concerns. The device is classified as a Class I recall, indicating a serious issue with potential for harm. The recall affects all TiLoop Mesh products in Canadian distribution.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-04-24
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ae6fbb4f-ee88-47ad-9dec-0f4c320d8b06