Health product recall

Excor System Cannulas

Last updated

Summary

Product
Excor System Cannulas
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Excor System - Apex Cannulas

All lots.

C14A-040M
C18A-020
C22A-004
C27A-001

Excor System - Atrial Cannulas

All lots.

C15V-040M
C23V-004
C25V-004
C22V-002M
C19V-020M
C22V-004

Excor System - Arterial Cannulas

All lots.

C60G-002M
C85G-004
C80G-040M
C85G-002M
C60G-004M
C80G-021M

Excor System - Connecting Set For Cannulas

All lots.

A06-009
A09-012

Issue

The purpose of the urgent medical device correction notification is to advise healthcare professionals that Berlin Heart is conducting a voluntary correction concerning all Excor cannulae due to the potential of partial or complete breaches of an Excor cannula. A significant cannula breach may result in massive blood loss and/or an air embolism which could result in blood loss and/or death to the patient.  No product will be removed.

Recall Start Date: August 4, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Berlin Heart gmbh

Wiesenweg 10, Berlin, Germany, 12247

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-74133

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