AtriClip® PRO•V™ LAA Exclusion System PROV45 (REF A000973-4)Recalls & reported problems
Atricure, Inc. · AtriClip® PRO•V™ LAA Exclusion System 45 · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10840143907647), received between Aug 22, 2024 and Aug 22, 2024 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Cardiac Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 22, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A PATIENT UNDERWENT A CONVERGENT PROCEDURE WITH CONCOMITANT VIDEO-ASSISTED THORACOSCOPIC (VATS) LEFT ATRIAL APPENDAGE EXCLUSION (LAAE) USING A PROV45 ATRICLIP DEVICE. DURING PLACEMENT OF THE CLIP DEVICE, AN INJURY OCCURRED AT THE BASE OF THE LEFT ATRIAL APPENDAGE (LAA). THE PROCEDURE WAS CONVERTED TO STERNOTOMY AND THE INJURY WAS REPAIRED WITH SUTURE. THE PROV45 WAS THEN SUCCESSFULLY PLACED AT THE BASE OF THE LAA. THE PATIENT IS REPORTEDLY RECOVERING. THERE WAS NO REPORTED DEVICE MALFUNCTION, AND THE ADVERSE EVENT WAS THE RESULT OF A PROCEDURAL COMPLICATION.
Patient problems: Cardiac Perforation
MAUDE report 20043425 ↗
Other Left Atrial Appendage Clip, Implantable devices
- Penditure™ LAAC45Medtronic, Inc. · Left atrial appendage clip, implantable7 reports
- Penditure™ LAAC50Medtronic, Inc. · Left atrial appendage clip, implantable1 death7 reports
- Penditure™ LAAC40Medtronic, Inc. · Left atrial appendage clip, implantable6 reports
- Penditure™ LAAC35Medtronic, Inc. · Left atrial appendage clip, implantable2 reports
- AtriClip PROV® LAA Exclusion System PROV50Atricure, Inc. · Left Atrial Appendage Clip, Implantable1 death1 report
- AtriClip® FLEX-Mini™ LAA Exclusion System ACHM50Atricure, Inc. · Left Atrial Appendage Clip, Implantable1 report
- AtriClip PRO2® Gillinov-Cosgrove™ LAA Exclusion System PRO235Atricure, Inc. · Left Atrial Appendage Clip, Implantable1 report
- AtriClip® FLEX-Mini™ LAA Exclusion System ACHM40Atricure, Inc. · Left Atrial Appendage Clip, Implantable1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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