FDA Adverse Event Injury Summary report: N

KIT IMPLANTABLE SLIM TIP LEAD, 50CM

MDR report key: 20392971 · Received October 7, 2024

Report

Report Number
1627487-2024-11366
Event Type
Injury
Date Received
October 7, 2024
Date of Event
September 17, 2024
Report Date
October 7, 2024
Manufacturer
ABBOTT MEDICAL
Product Code
PMP
UDI-DI
05415067027153
PMA / PMN Number
P150004
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

B3-DATE OF EVENT IS ESTIMATED. ADDITIONAL COMPONENTS POTENTIALLY INVOLVED IN THE EVENT INCLUDE: ADDITIONAL COMPONENTS POTENTIALLY INVOLVED IN THE EVENT: COMMON DEVICE NAME: DRG: LEAD, MODEL: MN20450-50A, UDI: (B)(4), SERIAL:(B)(6), BATCH: 7982307 COMMON DEVICE NAME: DRG: LEAD, MODEL: MN20450-50A, UDI: (B)(4), SERIAL:(B)(6), BATCH: 7982304 A PATIENT EXPERIENCING HIGH IMPEDANCE WAS REPORTED TO ABBOTT. THE PATIENT LEADS WERE EXPLANTED AND REPLACED. THERAPY WAS RESTORED. THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICES WERE NOT RETURNED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED.

Description of Event or Problem · 0

IT WAS REPORTED THAT PATIENT EXPERIENCED INEFFECTIVE THERAPY. SYSTEM DIAGNOSTICS RECORDED HIGH IMPEDANCES ON THE LEFT T12 LEAD AND RIGHT S1 LEAD. AS A RESULT, SURGICAL INTERVENTION WAS UNDERTAKEN WHEREIN THE LEADS WERE EXPLANTED AND REPLACED. EFFECTIVE THERAPY WAS RESTORED POST OPERATIVELY. THE INVESTIGATION WAS UNABLE TO DETERMINE THE LEADS THAT WERE ASSOCIATED WITH THE ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2544051 KIT IMPLANTABLE SLIM TIP LEAD, 50CM DRG LEAD PMP ABBOTT MEDICAL MN10450-50A 7982304 05415067027153

Patients

Seq Age Sex Outcome Treatment
1 NA Male Other DRG IPG| DRG LEAD X2