FDA Adverse Event Injury Summary report: N

QUATTRODE LEAD WIDE SPACED, 30 CM

MDR report key: 22845901 · Received August 19, 2025

Report

Report Number
1627487-2025-04110
Event Type
Injury
Date Received
August 19, 2025
Date of Event
August 1, 2025
Report Date
September 22, 2025
Manufacturer
ABBOTT MEDICAL
Product Code
LGW
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

DATE OF EVENT IS ESTIMATED.

Additional Manufacturer Narrative · 0

CORRECTION: ADDITIONAL INFORMATION WAS OBTAINED INDICATING THAT ONLY THE L SO LEAD ERODED. AS SUCH, SURGICAL INTERVENTION TOOK PLACE WHEREIN THE SYSTEM WAS EXPLANTED TO ADDRESS THE ISSUE. INVESTIGATION WAS UNABLE TO DETERMINE WHICH LOT WAS THE LEFT LEAD. THIS DEVICE IS NO LONGER CONSIDERED REPORTABLE. THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE AS THE DEVICE WAS NOT RETURNED FOR EVALUATION. BASED ON THE INFORMATION RECEIVED, A SINGLE DEFINITIVE ROOT CAUSE FOR THE ISSUE ENCOUNTERED WAS UNABLE TO BE CONCLUSIVELY DETERMINED.

Description of Event or Problem · 0

IT WAS REPORTED THE PATIENT'S LEADS ARE CAUSING SORENESS DUE TO EROSION. THERE IS NO CONCERN OF INFECTION. SURGICAL INTERVENTION MAY TAKE PLACE AT A LATER DATE.

Description of Event or Problem · 0

ADDITIONAL INFORMATION WAS OBTAINED INDICATING THAT ONLY THE L SO LEAD ERODED. AS SUCH, SURGICAL INTERVENTION TOOK PLACE WHEREIN THE SYSTEM WAS EXPLANTED TO ADDRESS THE ISSUE. INVESTIGATION WAS UNABLE TO DETERMINE WHICH LOT WAS THE LEFT LEAD. THIS DEVICE IS NO LONGER CONSIDERED REPORTABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1436131 QUATTRODE LEAD WIDE SPACED, 30 CM SCS LEAD LGW ABBOTT MEDICAL 3163 3773645

Patients

Seq Age Sex Outcome Treatment
1 NA Female Other SCS ADAPTERX2| SCS IPG