FDA Adverse Event Injury Summary report: N

PRECISION®

MDR report key: 3193356 · Received June 27, 2013

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 Manufacturer Narrative · 1

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 Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

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.

Description of Event or Problem · 1

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