Ngiotouch Hand Controller Kit (2017-12-19)
Angiotouch Hand Controller Kit Recall The Angiotouch Hand Controller Kit is being recalled across Canada because it is classified as a medical device that does not meet regulatory requirements. This recall affects all units of this product that were distributed in Canada. The device was intended for use in medical procedures but failed to comply with required standards.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-01-08
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ae4929b1-6df0-48e8-9504-fd368df26b1f