MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-03-29 for STIMLOC 924256 manufactured by Medtronic Neuromodulation.
[142079854]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[142079855]
Information was received from a healthcare provider via a manufacturing representative. It was reported that prior to use of the burr hole cover the hcp tried to close the clip, however it did not work properly. Without pressing too hard the burr hole cap opened again. A new burr hole cap was used in place of the first and this one worked properly. The issue was resolved at the time of the report. There was no patient involved with the event. No further complications were reported or anticipated. Additional information was received from the rep and hcp stating there was no lead associated with the stimloc. The surgeon found out about the malfunction before implanting the stimloc.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3007566237-2019-00752 |
| MDR Report Key | 8466682 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2019-03-29 |
| Date of Report | 2019-07-08 |
| Date of Event | 2019-03-07 |
| Date Mfgr Received | 2019-07-03 |
| Device Manufacturer Date | 2018-10-01 |
| Date Added to Maude | 2019-03-29 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | LISA WOODWARD CLARK |
| Manufacturer Street | 7000 CENTRAL AVENUE NE RCW215 |
| Manufacturer City | MINNEAPOLIS MN 55432 |
| Manufacturer Country | US |
| Manufacturer Postal | 55432 |
| Manufacturer Phone | 7635263920 |
| Manufacturer G1 | MEDTRONIC NEUROMODULATION |
| Manufacturer Street | 800 53RD AVE NE |
| Manufacturer City | MINNEAPOLIS MN 554211200 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 554211200 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | STIMLOC |
| Generic Name | COVER, BURR HOLE |
| Product Code | GXR |
| Date Received | 2019-03-29 |
| Returned To Mfg | 2019-03-18 |
| Model Number | 924256 |
| Catalog Number | 924256 |
| Lot Number | 082227418A |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Manufacturer Address | 800 53RD AVE NE MINNEAPOLIS MN 554211200 US 554211200 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-03-29 |