MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-12-13 for ESTEEM 2001/7504/7004 902001003/907504003/907004003 manufactured by Envoy Medical Corporation.
[130215170]
Patient is experiencing a post-operative infection. Currently being treated with antibiotics and monitored, by physician. Device remains implanted and therefore was not returned to emc or evaluated per returned product evaluation process. Device evaluation summary: test results from device manufacturing and dhr were reviewed. All components in question passed all functional testing in production and passed quality inspections. No anomalies associated with sterilization of product. No device failures are alleged. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[130215171]
Envoy medical corp. (emc) was notified on 12/04/2018 of a post-operative infection identified in a patient. No skin/wound breakdown has occured. Patient is experiencing draining from a pe tube (placed by physician (b)(6) 2018). No device deficiencies are alleged. Patient/clinical history with emc: on (b)(6) 2018-- initial implant. On (b)(6) 2018-- activation of device. On 2018-12-04 -- emc notified of post-operative infection. Case review, at the request of the physician.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3004007782-2018-00014 |
| MDR Report Key | 8160374 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2018-12-13 |
| Date of Report | 2018-12-13 |
| Date of Event | 2018-12-04 |
| Device Manufacturer Date | 2017-11-14 |
| Date Added to Maude | 2018-12-13 |
| 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 |
| Manufacturer Contact | MR. MAKSIM TROFIMOVICH |
| Manufacturer Street | 4875 WHITE BEAR PARKWAY |
| Manufacturer City | WHITE BEAR LAKE MN 551108057 |
| Manufacturer Country | US |
| Manufacturer Postal | 551108057 |
| Manufacturer Phone | 6513618029 |
| Manufacturer G1 | ENVOY MEDICAL CORPORATION |
| Manufacturer Street | 4875 WHITE BEAR PARKWAY |
| Manufacturer City | WHITE BEAR LAKE MN 551108057 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 551108057 |
| Single Use | 3 |
| Remedial Action | NO |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ESTEEM |
| Generic Name | ESTEEM II, PRODUCT CODE: OAF |
| Product Code | OAF |
| Date Received | 2018-12-13 |
| Model Number | 2001/7504/7004 |
| Catalog Number | 902001003/907504003/907004003 |
| Lot Number | EMC0006217/6085/6173 |
| Device Expiration Date | 2018-11-14 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ENVOY MEDICAL CORPORATION |
| Manufacturer Address | 4875 WHITE BEAR PARKWAY WHITE BEAR LAKE MN 55110 US 55110 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2018-12-13 |