FDA Adverse Event Injury Summary report: N

KIT IMPLANTABLE SLIM TIP LEAD, 90CM

MDR report key: 15555534 · Received October 6, 2022

Report

Report Number
1627487-2022-05378
Event Type
Injury
Date Received
October 6, 2022
Date of Event
September 9, 2022
Report Date
December 23, 2022
Manufacturer
ABBOTT MEDICAL
Product Code
PMP
UDI-DI
05415067027160
PMA / PMN Number
P150004
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

DATE OF THE EVENT IS ESTIMATED. DURING PROCESSING OF THIS INCIDENT, ATTEMPTS WERE MADE TO OBTAIN COMPLETE PATIENT INFORMATION. THE ALLEGATION IS AGAINST 1 OF 3 LEADS; HOWEVER, IT IS UNKNOWN WHICH COMPONENTS, THEREFORE, ALL POTENTIAL COMPONENTS ARE BEING LISTED. ADDITIONAL COMPONENTS POTENTIALLY INVOLVED IN THE EVENT INCLUDE: COMMON DEVICE NAME: SCS LEAD, MODEL: MN10450-90A, UDI: (B)(4), SERIAL: (B)(4), BATCH: 8081547. COMMON DEVICE NAME: SCS LEAD, MODEL: MN10450-90A, UDI: (B)(4), SERIAL: (B)(4), BATCH: 8176651.

Additional Manufacturer Narrative · 0

THE REPORTED EVENT FOR UNCOMFORTABLE STIMULATION WAS NOT CONFIRMED. VISUAL INSPECTION OF THE LEAD DID NOT IDENTIFY ANY ANOMALIES. THE LEAD WAS FUNCTIONALLY TESTED AND PASSED ALL TESTING.

Description of Event or Problem · 0

RELATED MANUFACTURER REFERENCE NUMBER 1627487-2022-05379. IT WAS REPORTED THE PATIENT WAS EXPERIENCING UNCOMFORTABLE STIMULATION (ZAPPING) AT THE GROIN AND RIGHT LEG AND A WARM SENSATION AT THE IPG POCKET. AS SUCH, THE PATIENT UNDERWENT SURGICAL INTERVENTION WHERE THE SYSTEM WAS EXPLANTED TO ADDRESS THE ISSUES. INVESTIGATION WAS UNABLE TO DETERMINE WHICH OF THE DEVICES ATTRIBUTED TO THE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2555530 KIT IMPLANTABLE SLIM TIP LEAD, 90CM DRG SLIM TIP LEAD PMP ABBOTT MEDICAL MN10450-90A 7711397 05415067027160

Patients

Seq Age Sex Outcome Treatment
1 Female Other