FDA Adverse Event Injury Summary report: N

KIT IMPLANTABLE SLIM TIP LEAD, 90CM

MDR report key: 22452070 · Received July 8, 2025

Report

Report Number
1627487-2025-03395
Event Type
Injury
Date Received
July 8, 2025
Date of Event
March 7, 2025
Report Date
September 15, 2025
Manufacturer
ABBOTT MEDICAL
Product Code
PMP
UDI-DI
05415067027160
PMA / PMN Number
P150004
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

DATE OF EVENT IS ESTIMATED. SECTION A4: DURING PROCESSING OF THIS INCIDENT, ATTEMPTS WERE MADE TO OBTAIN COMPLETE PATIENT INFORMATION (WEIGHT); HOWEVER, NO FURTHER INFORMATION WAS RECEIVED. THE ALLEGATION IS AGAINST 2 OF 3 CERVICAL DRG LEADS; HOWEVER, IT IS UNKNOWN WHICH LEAD; THEREFORE, ALL POTENTIAL COMPONENTS ARE BEING LISTED. ADDITIONAL COMPONENTS POTENTIALLY INVOLVED IN THE EVENT INCLUDE: COMMON DEVICE NAME: KIT IMPLANTABLE SLIM TIP LEAD, 90CM, MODEL: MN10450-90A, UDI: (B)(4), SERIAL: (B)(6), BATCH: 6813185.

Additional Manufacturer Narrative · 0

THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICE WAS NOT RETURNED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE PATIENT WAS EXPERIENCING INEFFECTIVE THERAPY WITH THEIR DRG SYSTEM. DIAGNOSTICS INDICATED HIGH IMPEDANCES ON TWO OF THE CERVICAL DRG LEADS. AS A RESULT, SURGICAL INTERVENTION TOOK PLACE ON (B)(6) 2025, WHEREIN THE IMPEDED LEADS WERE EXPLANTED AND REPLACED TO ADDRESS THE ISSUE. IT IS UNKNOWN WHICH LEADS CAUSED THE ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
702331 KIT IMPLANTABLE SLIM TIP LEAD, 90CM DRG LEAD PMP ABBOTT MEDICAL MN10450-90A 6873392 05415067027160

Patients

Seq Age Sex Outcome Treatment
1 33 YR Female Other DRG IPG.| DRG LEAD.| DRG LEAD.