FDA Adverse Event
Injury
Summary report: N
INTERSTIM
MDR report key: 1250373
·
Received December 3, 2008
Report
- Report Number
- 2182207-2008-07953
- Event Type
- Injury
- Date Received
- December 3, 2008
- Report Date
- November 6, 2008
- Manufacturer
- MEDTRONIC NEUROMODULATION
- Product Code
- EZW
- PMA / PMN Number
- P970004
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
JOURNAL REFERENCE: FAUCHERON JL, BOST R, DUFFOURNET V, DUPUY S, CARDIN N, BONAZ B. SACRAL NEUROMODULATION IN THE TREATMENT OF SEVERE ANAL INCONTINENCE. FORTY CONSECUTIVE CASES TREATED IN ONE INSTITUTION. GASTROENTEROL CLIN BIOL. MAY 2006;30(5):669-672. SACRAL NEUROMODULATION IS A RECOGNIZED THERAPEUTIC OPTION IN SEVERE ANAL INCONTINENCE FROM NEUROGENIC ORIGINS, WHEN MEDICAL TREATMENT HAS FAILED. TWENTY NINE PATIENTS HAD A POSITIVE TEST AND WERE IMPLANTED. REPORTABLE EVENT: ONE PATIENT HAS A PERSISTENT SEROMA; A SIMPLE NEEDLE ASPIRATION WAS PERFORMED WITH STERILE RESULTS DURING THE FIRST MONTH FOLLOW UP VISIT. SEE MFG REPORT # 2182207200807948.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INTERSTIM | EZW | MEDTRONIC NEUROMODULATION | 3023 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention | EXTENSION: MODEL UNK N=1| LEAD: MODEL UNK N=1| PROGRAMMER: MODEL UNK N=1 |