S.m.a.r.t. Control Nitinol Stent (2019-11-13)

S.M.A.R.T. Control Nitinol Stent Recall The S.M.A.R.T. Control Nitinol Stent, a medical device used in vascular procedures, has been recalled across Canada. The specific reason for the recall relates to issues with the device itself, classified as a Class I recall, which is the most serious type. This recall affects patients and healthcare facilities throughout Canada who have received or may use this stent product.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-12-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2c3c2702-5de3-4abd-88ba-3b217a8bfad3