FDA Adverse Event Injury Summary report: N

OCTRODE LEAD KIT, 60CM LENGTH

MDR report key: 8640101 · Received May 24, 2019

Report

Report Number
3006705815-2019-01940
Event Type
Injury
Date Received
May 24, 2019
Date of Event
May 7, 2019
Report Date
June 26, 2019
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)
Product Code
LGW
UDI-DI
05415067017246
PMA / PMN Number
P010032
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

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.

Additional Manufacturer Narrative · 1

THE RESULTS/METHOD AND CONCLUSION CODES ALONG WITH INVESTIGATION RESULTS WILL BE PROVIDED IN THE FINAL REPORT.

Description of Event or Problem · 1

RELATED MANUFACTURER REFERENCE NUMBER: 3006705815-2019-01941RELATED MANUFACTURER REFERENCE NUMBER: 1627487-2019-06099.

Description of Event or Problem · 1

RELATED MFR. REPORT#: 3006705815-2019-001941. RELATED MFR. REPORT #:1627487-2019-06099. ADDITIONAL INFORMATION INDICATES SURGICAL INTERVENTION WAS UNDERTAKEN ON (B)(6) 2019 WHEREIN THE PATIENT'S SYSTEM WAS EXPLANTED.

Description of Event or Problem · 1

REFERENCE MANUFACTURER REPORT NUMBER: 3006705815-2019-01941, REFERENCE MANUFACTURER REPORT NUMBER: 1627487-2019-06099. IT WAS REPORTED THAT THE PATIENT WAS EXPERIENCING INEFFECTIVE THERAPY. SURGICAL INTERVENTION MAY BE PENDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
434555 OCTRODE LEAD KIT, 60CM LENGTH SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC) 3186 A000053919 05415067017246

Patients

Seq Age Sex Outcome Treatment
1 Other MODEL: 3186, SCS LEAD| MODEL: 3662, SCS IPG