Public recall detail

Amplatzer™ Amulet™ Left Atrial Appendage Occluder

2026-09-25

medium
Health products Health product recall
Quick summary

Quick summary: Amplatzer™ Amulet™ Left Atrial Appendage Occluder. Reason: Health product recall. Category: Health products. Date: 2026-09-25.

Recommended action

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.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandABBOTT MEDICAL
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-82682

Affected products

ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-010-028
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-010-031
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-010-034
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-007-020
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-007-022
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-007-016
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-007-018
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder
ProductAmplatzer™ Amulet™ Left Atrial Appendage Occluder
LotMore than 10 numbers, contact manufacturer.
Model9-ACP2-010-025
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAmplatzer™ Amulet™ Left Atrial Appendage Occluder

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
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesAbbott Medical 5050 Nathan Lane North, Plymouth, Minnesota, United States, 55442
Recall date2026-09-10
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82682
Background{}
CompaniesAbbott Medical 5050 Nathan Lane North, Plymouth, Minnesota, United States, 55442
AudiencesHealthcare
Source updated2026-09-25

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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