MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-27 for NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADVANCE ELECTRODE CI24RE (CA) NA manufactured by Cochlear Ltd.
[186271524]
This report is submitted on march 27, 2020.
Patient Sequence No: 1, Text Type: N, H10
[186271525]
Per the surgeon, the patient experienced skin breakdown resulting in the implant extruding. The implant was successfully re-positioned (date unknown).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6000034-2020-00865 |
| MDR Report Key | 9887251 |
| Date Received | 2020-03-27 |
| Date of Report | 2020-03-04 |
| Report Date | 2020-03-27 |
| Date Reported to FDA | 2020-03-27 |
| Date Reported to Mfgr | 2020-03-04 |
| Date Mfgr Received | 2020-03-04 |
| Device Manufacturer Date | 2012-05-04 |
| Date Added to Maude | 2020-03-27 |
| 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 | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADVANCE ELECTRODE |
| Generic Name | NUCLEUS 24 COCHLEAR IMPLANT SYSTEM |
| Product Code | MCM |
| Date Received | 2020-03-27 |
| Model Number | CI24RE (CA) |
| Catalog Number | NA |
| Lot Number | NA |
| Device Expiration Date | 2014-05-03 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COCHLEAR LTD |
| Manufacturer Address | 1 UNIVERSITY AVENUE MACQUARIE UNIVERSITY, 2109 AS 2109 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-03-27 |