PRECISION®
Report
- Report Number
- 3006630150-2013-01332
- Event Type
- Injury
- Date Received
- June 27, 2013
- Date of Event
- April 25, 2013
- Report Date
- June 6, 2013
- Manufacturer
- BOSTON SCIENTIFIC NEUROMODULATION
- Product Code
- LGW
- PMA / PMN Number
- 030017
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OK, US
- Reporter Occupation
- PHYSICIAN
Narratives
ADDITIONAL INFORMATION WAS RECEIVED THAT THE PATIENT UNDERWENT AN EXPLANT PROCEDURE. THE EXPLANTED DEVICES WERE NOT RETURNED TO BSN AS THEY WERE DISCARDED BY THE MEDICAL FACILITY. IT IS INDICATED THAT THE DEVICES WILL NOT BE RETURNED FOR EVALUATION; THEREFORE A FAILURE ANALYSIS OF THE COMPLAINT DEVICES COULD NOT BE COMPLETED. A REVIEW OF THE DEVICE HISTORY RECORDS WILL BE CONDUCTED. IF THERE IS ANY FURTHER RELEVANT INFORMATION FROM THAT REVIEW, A SUPPLEMENTAL MED WATCH WILL BE FILED.
ADDITIONAL SUSPECT MEDICAL DEVICE COMPONENTS INVOLVED IN THE EVENT: MODEL #: SC-2352-70, SERIAL/LOT #: (B)(4), DESCRIPTION: LINEAR 3-4 LEAD, 70CM. MODEL #: SC-3138-35, SERIAL/LOT #: (B)(4), DESCRIPTION: SCS PHIII EXT 35CM.
A REPORT WAS RECEIVED THAT THE PATIENT WAS EXPERIENCING NAUSEA AND DIARRHEA WHICH IS RELATED TO THE STIMULATION. THE PATIENT WILL UNDERGO AN EXPLANT PROCEDURE.
A REPORT WAS RECEIVED THAT THE PATIENT WAS EXPERIENCING NAUSEA AND DIARRHEA WHICH IS RELATED TO THE STIMULATION. THE PATIENT WILL UNDERGO AN EXPLANT PROCEDURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 293727 | PRECISION® | SPINAL CORD STIMULATOR | LGW | BOSTON SCIENTIFIC NEUROMODULATION | SC-1110-02 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 37 YR | Required Intervention |