FDA Adverse Event Injury Summary report: N

INTERSTIM II

MDR report key: 5953257 · Received September 15, 2016

Report

Report Number
3007566237-2016-03276
Event Type
Injury
Date Received
September 15, 2016
Date of Event
June 13, 2016
Report Date
September 15, 2016
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
EZW
PMA / PMN Number
P080025
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NL
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

IT WAS NOT POSSIBLE TO ASCERTAIN SPECIFIC DEVICE INFORMATION FROM THE ARTICLE OR TO MATCH THE EVENTS REPORTED WITH PREVIOUSLY REPORTED EVENTS. THE DEVICE WAS USED FOR AN OFF LABEL INDICATION. OTHER APPLICABLE COMPONENTS ARE: PRODUCT ID: 3889, PRODUCT TYPE: LEAD.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

VAN DER WILT, A.A., VAN WUNNIK, B.P., STURKENBOOM, R., HAN-GEURTS, I.J., MELENHORST, J., BENNINGA, M.A., BAETEN, C.G.M.I., BREUKINK, S.O. SACRAL NEUROMODULATION IN CHILDREN AND ADOLESCENTS WITH CHRONIC CONSTIPATION REFRACTORY TO CONSERVATIVE TREATMENT. INT. J. COLORECTAL DIS. 2016. 31(8):1459-1466. DOI 10.1007/S00384-016-2604-8. SUMMARY: THE AIM OF THIS STUDY WAS TO EVALUATE WHETHER THE SHORT-TERM EFFECTS OF SACRAL NEUROMODULATION (SNM) IN CHILDREN AND ADOLESCENTS WITH CONSTIPATION ARE SUSTAINED OVER PROLONGED PERIOD OF TIME. REPORTED EVENTS: PATIENT 28: A (B)(6) FEMALE PATIENT WITH SACRAL NEUROMODULATION (SNM) FOR REFRACTORY CONSTIPATION HAD THEIR ELECTRODE REMOVED WITHIN A YEAR POST-IMPLANT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
606669 INTERSTIM II STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE EZW MEDTRONIC NEUROMODULATION 3058 UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 15 YR Required Intervention