Precise Pro Rx Nitinol Stent System (2016-05-06)

Recall Summary Precise Pro Rx Nitinol Stent Systems are being recalled across Canada due to a medical device issue. The recall is classified as Class I, meaning there is a serious potential health risk associated with the product. This recall affects stent systems that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-05-24

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/380cdb21-3e51-4187-9a82-83dc398c6e58