MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION ENDOTAK RELIANCE; IMPLANTABLE LEAD

Model Number	0158
Medical Device Problem Code	High impedance (1291)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/08/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
At this time, no further information is available.Should additional information become available this report will be updated.
Event or Problem Description
It was reported that this implantable cardioverter defibrillator (icd) system exhibited high out of range pacing impedance measurements on the right ventricular (rv) lead.Further monitoring was recommended.No adverse patient effects were reported.This rv lead remains in service.
Event or Problem Description
It was reported that this implantable cardioverter defibrillator (icd) system exhibited high out of range pacing impedance measurements on the right ventricular (rv) lead.Further monitoring was recommended.No adverse patient effects were reported.This rv lead remains in service.Additional information indicated that technical services (ts) suspected possible spring contact abnormally.No adverse patient effects were reported.This rv lead remains in service.
Additional Manufacturer Narrative
Follow up 1 (additional information) this report is being submitted to update section b5.At this time, no further information is available.Should additional information become available this report will be updated.

• Brand Name: ENDOTAK RELIANCE
• Common Device Name: IMPLANTABLE LEAD
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 4100 hamline avenue north; saint paul MN 55112
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; road 698, lot no. 12; dorado PR 00646 -260; * 00646-2602
• Manufacturer Contact: timothy degroot ; 4100 hamline avenue north; saint paul, MN 55112 ; 6515826168
• MDR Report Key: 22911173
• Report Number: 2124215-2025-60475
• Device Sequence Number: 18424593
• Product Code: LWS
• UDI-Device Identifier: 00802526531132
• UDI-Public: (01)00802526531132(17)230517
• Combination Product (Y/N): Y
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: P910073
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 12/01/2025

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: Lay User/Patient
• Device Expiration Date: 05/17/2023
• Device Model Number: 0158
• Device Catalogue Number: 0158
• Device Lot Number: 316757
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/11/2025
• Supplement Date Received by Manufacturer: 11/26/2025
• Initial Report FDA Received Date: 08/28/2025
• Supplement Report FDA Received Date: 12/01/2025
• Date Device Manufactured: 05/17/2021
• 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 Age: 65 YR
• Patient Sex: Male