Waterlase Express All-tissue Laser System
Waterlase Express All-Tissue Laser System Recall The Waterlase Express All-Tissue Laser System, a medical device used in dental and surgical procedures, is being recalled across Canada. The FDA classified this as a Class I recall, indicating a serious safety concern. The recall affects all units of this laser system that were distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-06-21
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/273d77c3-06f6-4e32-8bc5-9277c73b3bbb