MAUDE Adverse Event Report: ABBOTT MEDICAL AMPLATZER MUSCULAR VSD OCCLUDER; TRANSCATHETER SEPTAL OCCLUDER

Model Number	VSD MUSCULAR OCCLUDER
Medical Device Problem Code	Migration or Expulsion of Device (1395)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/14/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that a 10mm amplatzer vsd muscular occluder and 12mm amplatzer vsd muscular occluder were selected from an implant on 14 june 2022.The defect was sized using echocardiogram.During the procedure, it was reported that 10mm and 12mm amplatzer vsd occluder shifted within the intended implant site towards the left ventricle.It is unknown what caused the devices to shift in position.Patient was sent to emergent open heart surgery to retrieve the occluder.No replacement device was implanted.
Additional Manufacturer Narrative
Investigation is not yet complete.A follow-up report will be submitted with all additional relevant information.
Event or Problem Description
It was reported that a 10mm amplatzer vsd muscular occluder and 12mm amplatzer vsd muscular occluder were selected from an implant on (b)(6) 2022.The defect was sized using echocardiogram.During the procedure, it was reported that 10mm and 12mm amplatzer vsd occluder shifted within the intended implant site towards the left ventricle.It is unknown what caused the devices to shift in position.Patient was sent to emergent open heart surgery to retrieve the occluder.No replacement device was implanted.Subsequent to the previously filed report, additional information was received.It was reported that the patient had a challenging anatomy.
Additional Manufacturer Narrative
An event of device shifted within the intended implant site towards the left ventricle was reported.A returned device assessment could not be performed as the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
Additional Manufacturer Narrative
An event of device shifted within the intended implant site towards the left ventricle was reported.A returned device assessment could not be performed as the device was not returned for analysis.The device history record was reviewed to ensure that each manufacturing and inspection operation was performed and the product met all specifications.Based on the information received, the cause of the reported incident could not be conclusively determined.
Additional Manufacturer Narrative
Naincorrect device originally reported.The correct device was a 9-vsd-musc-008.D4: corrected-lot number, catalog number, expiration date, udi.H4: corrected manufacturing date.

• Brand Name: AMPLATZER MUSCULAR VSD OCCLUDER
• Common Device Name: TRANSCATHETER SEPTAL OCCLUDER
• Manufacturer (Section D): ABBOTT MEDICAL; 5050 nathan lane n; plymouth MN 55442
• Manufacturer (Section G): ABBOTT MEDICAL REG# 2135147; 5050 nathan ln n; plymouth MN 55442
• Manufacturer Contact: karen krouse ; 5050 nathan lane n; plymouth, MN 55442 ; 6517565400
• MDR Report Key: 14991568
• Report Number: 2135147-2022-00489
• Device Sequence Number: 16588513
• Product Code: MLV
• UDI-Device Identifier: 00811806011806
• UDI-Public: 00811806011806
• Combination Product (Y/N): N
• Initial Reporter Country: IN
• PMA/510(K) Number: P040040
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 01/10/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 06/30/2024
• Device Model Number: VSD MUSCULAR OCCLUDER
• Device Catalogue Number: 9-VSD-MUSC-008
• Device Lot Number: 7085062
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 06/14/2022
• Supplement Date Received by Manufacturer: 11/17/2022; 01/10/2023; 01/10/2023
• Initial Report FDA Received Date: 07/12/2022
• Supplement Report FDA Received Date: 11/25/2022; 01/10/2023; 01/10/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 07/12/2019
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 59 YR
• Patient Sex: Male