MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2009-03-03 for INTERSTIM 3023 NA manufactured by Medtronic Puerto Rico Operations Co..
        [1068441]
The patient experienced shocking / jolting sensations from her device. Turning the stimulation down resulted in loss of therapeutic effect. Further information is being requested from the hcp.
 Patient Sequence No: 1, Text Type: D, B5
        [8179349]
.
 Patient Sequence No: 1, Text Type: N, H10
| Report Number | 3004209178-2009-01483 | 
| MDR Report Key | 1358044 | 
| Report Source | 04 | 
| Date Received | 2009-03-03 | 
| Date of Report | 2009-02-05 | 
| Date Mfgr Received | 2009-02-05 | 
| Device Manufacturer Date | 2006-10-04 | 
| Date Added to Maude | 2009-06-30 | 
| Event Key | 0 | 
| Report Source Code | Manufacturer report | 
| Manufacturer Link | Y | 
| Number of Patients in Event | 0 | 
| Adverse Event Flag | 3 | 
| Product Problem Flag | 3 | 
| Reprocessed and Reused Flag | 3 | 
| Health Professional | 3 | 
| Initial Report to FDA | 3 | 
| Report to FDA | 0 | 
| Event Location | 3 | 
| Manufacturer Contact | CHARLOTTE GASPERLIN | 
| Manufacturer Street | 7000 CENTRAL AVE. | 
| Manufacturer City | MINNEAPOLIS MN 554323576 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 554323576 | 
| Manufacturer Phone | 7635263952 | 
| Manufacturer G1 | MEDTRONIC PUERTO RICO OPERATIONS CO. | 
| Manufacturer Street | ROAD #31, KM. 24, HM 4 CEIBA NORTE INDUSTRIAL PARK | 
| Manufacturer City | JUNCOS PR 00777 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 00777 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | INTERSTIM | 
| Product Code | EZM | 
| Date Received | 2009-03-03 | 
| Model Number | 3023 | 
| Catalog Number | NA | 
| Lot Number | NA | 
| ID Number | NA | 
| Device Expiration Date | 2008-03-28 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| Device Age | NA | 
| Device Eval'ed by Mfgr | R | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. | 
| Manufacturer Address | ROAD #31, KM. 24, HM 4 CEIBA NORTE INDUSTRIAL PARK JUNCOS PR 00777 US 00777 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2009-03-03 |