Health product recall

Heartmate 3 LVAS Implant Kit

Last updated

Summary

Product
Heartmate 3 LVAS Implant Kit
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

Heartmate 3 LVAS Implant Kit

More than 10 numbers, contact manufacturer.

106524
106524US

Issue

There have been complaints of blood leaking out of the left ventricle or air entering the left ventricle or Left Ventricle Assist Device (LVAD) which are attributed to a leak path at the seal interface between the Heartmate 3 Left Ventricle Assist System (LVAS) inflow cannula and the titanium apical cuff. The blood leak or air entrainment has only been observed during the implantation procedure. Once the bleeding or air entrainment was resolved intraoperatively, the issue did not re-occur postoperatively. Abbott's investigation determined that in certain instances, routine manipulation of the pump or internal fluid pressures during implantation can result in a compressed sealing ring on one side, leading to a leak path on the opposite side.

Recall Start Date: March 19, 2024

Additional information

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

Thoratec Corporation

6035 Stoneridge Drive, Pleasanton, California, United States, 94588

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-75348

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