OCTRODE LEAD KIT, 60CM LENGTH
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
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.
THE RESULTS/METHOD AND CONCLUSION CODES ALONG WITH INVESTIGATION RESULTS WILL BE PROVIDED IN THE FINAL REPORT.
RELATED MANUFACTURER REFERENCE NUMBER: 3006705815-2019-01941RELATED MANUFACTURER REFERENCE NUMBER: 1627487-2019-06099.
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.
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 |