MAUDE Adverse Event Report: ABBOTT MEDICAL AMPLATZER VASCULAR PLUG 4; DEVICE, VASCULAR, FOR PROMOTING EMBOLIZATION

Catalog Number	9-AVP038-007
Medical Device Problem Codes	Migration or Expulsion of Device (1395); Off-Label Use (1494)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/14/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
The article, ¿risk factors associated with device embolisation or malposition during transcatheter closure of patent ductus arteriosus¿, was reviewed.The article presented a case study of a 3 month old patient weighing 2.2 kg that was born pre-term.It was reported that on an unknown date, an 7mm amplatzer vascular plug iv was chosen for implant to treat patent ductus arteriosus (pda) that was sized 5 mm.It was then reported on an unknown date, the device had embolized and a decision was made to retrieve the device via transcatheter snare and replace with a 8mm amplatzer vascular plug ii.The article concluded device embolisation complicates 4% of transcatheter duct closures, with need for surgery in one-fifth of them.Larger ducts with high pulmonary artery pressures in younger and smaller infants are more often associated with device embolisation.Tubular ducts are more prone for embolisation compared to usual conical ducts.Softer vascular plugs are often associated with embolisations.Intentional device undersizing to avoid vascular obstruction in small patients is a frequent risk factor for embolisation.Precise echocardiographic measurements, correct occluder choice, proper technique and additional care in patients with high pulmonary artery pressures are mandatory to minimise embolisations.[the primary and secondary author was kothandam sivakumar, madras medical mission, 4a dr jj nagar, mogappair, chennai 600089, india, with corresponding email drkumarsiva@hotmail.Com].
Additional Manufacturer Narrative
Investigation is not yet complete.A follow-up report will be submitted with all additional relevant information.
Additional Manufacturer Narrative
As reported in a research article, risk factors associated with device embolisation or malposition during transcatheter closure of patent ductus arteriosus.A more comprehensive assessment could not be performed as the event was non-contemporaneously reported through a literature review and no device was received for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.

• Brand Name: AMPLATZER VASCULAR PLUG 4
• Common Device Name: DEVICE, VASCULAR, FOR PROMOTING EMBOLIZATION
• 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: 18278817
• Report Number: 2135147-2023-05351
• Device Sequence Number: 6667888
• Product Code: KRD
• UDI-Device Identifier: 00811806012377
• UDI-Public: 00811806012377
• Combination Product (Y/N): N
• Initial Reporter Country: IN
• PMA/510(K) Number: K113658
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• 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
• Report Date (Section B): 12/28/2023

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?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 9-AVP038-007
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 11/13/2023
• Supplement Date Received by Manufacturer: 12/07/2023
• Initial Report FDA Received Date: 12/06/2023
• Supplement Report FDA Received Date: 12/29/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• 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: 3 MO
• Patient Sex: Unknown
• Patient Weight: 2 KG