MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION INTERLOCK?; DEVICE, VASCULAR, FOR PROMOTING EMBOLIZATION

Model Number	M001361740
Medical Device Problem Codes	Separation Failure (2547); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/23/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Device evaluated by mfr: only the introducer sheath and the pusher wire were returned for evaluation.It was observed that the pusher wire was kinked at the interlocking arm coil and detached at the heat shrink tfe tubing.There is a picture attached in the parent record, it was possible to observed that the pusher wire was kinked and detached.No other issues were identified during the product analysis.
Event or Problem Description
Reportable based on device analysis completed on 30dec2025.It was reported that the coil did not deploy.The non stenosed target lesion was located in a non-tortuous and non-calcified vessel of prostate.A 2/3mm x 2.3cm interlock was selected for use.During the procedure, it was noted that the coil got stuck and did not deploy.The coil was removed and the procedure was completed with another of the same device.There were no patient complications as a result of this event.However, device analysis revealed detached pusher wire.

• Brand Name: INTERLOCK?
• Common Device Name: DEVICE, VASCULAR, FOR PROMOTING EMBOLIZATION
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; model farm road; cork T12 Y K88; EI T12 YK88
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 24179468
• Report Number: 2124215-2026-04464
• Device Sequence Number: 15845390
• Product Code: KRD
• UDI-Device Identifier: 08714729765080
• UDI-Public: (01)08714729765080(17)271222(10)35672739
• Combination Product (Y/N): N
• Initial Reporter Country: MX
• PMA/510(K) Number: K132578
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 01/26/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: M001361740
• Device Catalogue Number: M001361740
• Device Lot Number: 0035672739
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/26/2025
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/30/2025
• Initial Report FDA Received Date: 01/26/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/21/2025
• 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
• Patient Sex: Unknown