Osstell® Smartpeg Type 101-104

Osstell® Smartpeg Type 101-104 Recall Summary Osstell® Smartpeg Type 101-104 devices are being recalled in Canada due to performance issues. The devices are used in dental applications and classified as a Class I recall, indicating a serious safety concern. The recall affects all units distributed across Canada.

Product
Osstell® Smartpeg Type 101-104
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-07-17
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/382727bb-628d-4197-80c9-8e7aa3552cf0