Reprocessed Diagnostic Electrophysiology (ep) Catheters (2018-01-25)

Recall Summary Reprocessed diagnostic electrophysiology catheters used in heart procedures have been recalled across Canada due to safety concerns with how they were reprocessed for reuse. This Class I recall indicates a serious potential health risk. The affected catheters were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-02-09

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d4b3d4fa-4415-47d0-be22-bd7980f2b3b9