FDA Adverse Event Injury Summary report: N

IPG

MDR report key: 1082556 · Received July 25, 2008

Report

Report Number
2182207-2008-04382
Event Type
Injury
Date Received
July 25, 2008
Report Date
July 1, 2008
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
EZW
PMA / PMN Number
P970004
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

SEE SCANNED PAGES.

Description of Event or Problem · 1

JOURNAL REFERENCE: KESSLER, T.M., ET AL., "SACRAL NEUROMODULATION FOR REFRACTORY LOWER URINARY TRACT DYSFUNCTION: RESULTS OF A NATIONWIDE REGISTRY IN A FOREIGN COUNTRY" EUROPEAN UROLOGY, (2007) 51: 1357-63. THE ARTICLE DISCUSSES THE TREATMENTS AND OUTCOME OF 209 PATIENTS. ADVERSE EVENTS WERE RECORDED DURING THE INITIAL TST PHASE AND/OR DURING OR FOLLOWING TRADITIONAL ONE-STAGE TECHNIQUE. REPORTABLE EVENT: AFTER THE IMPLANT OF THE IPG, ONE PT EXPERIENCED THE IPG MALFUNCTIONING AFTER AN MRI PROCEDURE. SURGICAL INTERVENTION WITH REPLACEMENT WAS PERFORMED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IPG EZW MEDTRONIC NEUROMODULATION UNK NA

Patients

Seq Age Sex Outcome Treatment
1 UNK Required Intervention PROGRAMMER MODEL UNK N=1| LEAD MODEL UNK N=1