Reprocessed Daig Supreme And Response Electrophysiology Catheters (2016-04-28)

Recall Summary Reprocessed DAIG Supreme and Response electrophysiology catheters have been recalled across Canada due to concerns with the medical devices themselves. These catheters are used in heart rhythm procedures and were distributed nationwide. This is classified as a Class I recall, indicating a serious safety issue.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-05-16
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c676b6f5-09c8-4aa0-81b4-88ec13a1d50c