PRECISION®
Report
- Report Number
- 3006630150-2011-00883
- Event Type
- Injury
- Date Received
- June 10, 2011
- Date of Event
- May 18, 2011
- Report Date
- May 18, 2011
- Manufacturer
- BOSTON SCIENTIFIC NEUROMODULATION
- Product Code
- LGW
- PMA / PMN Number
- 030017
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
ADDITIONAL SUSPECT MEDICAL DEVICE COMPONENTS INVOLVED IN THE EVENT: MODEL# SC-8216-70, (B)(4), DESCRIPTION:ARTISAN 2X8 PADDLE LEAD (LIM), 70 CM THE EXPLANTED DEVICES WERE NOT RETURNED TO BSN FOR EVALUATION AS THEY WERE DISCARDED BY THE MEDICAL FACILITY.
A REVIEW OF THE MANUFACTURING DOCUMENTATION OF THE EXPLANTED DEVICES REVEALED NO ANOMALIES OR DEVIATIONS POTENTIALLY RELATED TO THE REPORTED EVENT OCCURRED DURING MANUFACTURING. A REVIEW OF THE STERILIZATION DOCUMENTATION FOUND THEM TO BE SATISFACTORY.
A REPORT WAS RECEIVED THAT A PATIENT¿S PRECISION SYSTEM WAS EXPLANTED DUE TO AN INFECTION AT THE POCKET SITE. THE PATIENT WAS PLACED ON IV ANTIBIOTICS. THE PHYSICIAN BELIEVES THE INFECTION WAS NOT DEVICE OR PROCEDURE RELATED AS THE PATIENT WAS DIABETIC. THE PATIENT IS REPORTEDLY DOING WELL FOLLOWING THE PROCEDURE.
A REPORT WAS RECEIVED THAT A PATIENT'S PRECISION SYSTEM WAS EXPLANTED DUE TO AN INFECTION AT THE POCKET SITE. THE PATIENT WAS PLACED ON IV ANTIBIOTICS. THE PHYSICIAN BELIEVES THE INFECTION WAS NOT DEVICE OR PROCEDURE RELATED AS THE PATIENT WAS DIABETIC. THE PATIENT IS REPORTEDLY DOING WELL FOLLOWING THE PROCEDURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PRECISION® | SPINAL CORD STIMULATOR | LGW | BOSTON SCIENTIFIC NEUROMODULATION | SC-1110-02 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |