MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-12-18 for MICROTARGETING ELECTRODE 5005L manufactured by Fhc.
[34329571]
The targeting electrodes produced by fhc (specifically the thick tube and the guidewire) caused increased impedances and prolonged the surgical procedure because they have to be replaced.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5058696 |
| MDR Report Key | 5324353 |
| Date Received | 2015-12-18 |
| Date of Report | 2015-12-18 |
| Date of Event | 2015-12-18 |
| Date Added to Maude | 2015-12-23 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | MICROTARGETING ELECTRODE |
| Generic Name | MICROTARGETING ELECTRODE |
| Product Code | GZL |
| Date Received | 2015-12-18 |
| Returned To Mfg | 2015-12-21 |
| Model Number | 5005L |
| Catalog Number | 5005L |
| Lot Number | 211561 |
| Device Expiration Date | 2018-01-01 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | FHC |
| Manufacturer Address | 1201 MAIN ST. BOWDOIN ME 04287 US 04287 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2015-12-18 |