Reprocessed Ep Catheter (2018-03-29)

Reprocessed EP Catheter Recall Summary A reprocessed EP catheter (a medical device used in heart procedures) is being recalled across Canada due to safety concerns. The device was classified as a Class I recall, indicating a serious issue with the product. The recall affects medical facilities and healthcare providers that received this device for use in patient care.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-05-11

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3f48987d-3343-4823-aa22-f8a6064f723f