Health product recall

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

Brand(s)
Last updated

Summary

Product
Amplatzer™ Amulet™ Left Atrial Appendage Occluder
Issue
Medical devices - Labelling and packaging
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected product

Lot or serial number

Model or catalogue number

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-010-028

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-010-031

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-010-034

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-007-020

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-007-022

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-007-016

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-007-018

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

More than 10 numbers, contact manufacturer.

9-ACP2-010-025

Issue

The current Amulet™ IFU contains a contraindication against use "where placement of the device would interfere with any intracardiac or intravascular structures." Abbott is updating this contraindication to specifically identify the pulmonary artery as one of the adjacent structures. In addition, Abbott is updating the IFU to include additional guidance about assessing the distance between the device landing zone and the pulmonary artery. Abbott recently completed additional physician training on this subject.

For clarification, this recall is not associated with defectiveness or possible defectiveness. Abbott is informing consignees about changes to the instructions for use (IFU) for the Amplatzer™ Amulet™ Left Atrial Appendage Occluder (referred to as Amulet™) regarding pulmonary artery injury (PAI).

Additional information

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

Abbott Medical

5050 Nathan Lane North, Plymouth, Minnesota, United States, 55442

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82682

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