Quick summary: Amplatzer™ Amulet™ Left Atrial Appendage Occluder. Reason: Health product recall. Category: Health products. Date: 2026-09-25.
Amplatzer™ Amulet™ Left Atrial Appendage Occluder
2026-09-25
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Amplatzer™ Amulet™ Left Atrial Appendage Occluder. Reason: Health product recall. Category: Health products. Date: 2026-09-25.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
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).
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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