MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-21 for PATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS TYY-NNNNM manufactured by Tmj Solutions, Inc..
[176241798]
This patient received bilateral tmj implants in (b)(6) 2018. Approximately a year after implantation, the patient started experiencing swelling on the left side. On (b)(6) 2019, the surgeon removed the patient's left tmj devices and placed an antibiotic spacer. The surgeon plans on placing revision components after the infection has been resolved.
Patient Sequence No: 1, Text Type: N, H10
[176241799]
The patient's left tmj devices were removed due to infection.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2031049-2020-00002 |
| MDR Report Key | 9611776 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2020-01-21 |
| Date of Report | 2020-01-21 |
| Date of Event | 2019-12-17 |
| Date Mfgr Received | 2019-12-17 |
| Device Manufacturer Date | 2018-06-01 |
| Date Added to Maude | 2020-01-21 |
| 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 | MS. LORENA LUNDEEN |
| Manufacturer Street | 6059 KING DRIVE |
| Manufacturer City | VENTURA CA 930037398 |
| Manufacturer Country | US |
| Manufacturer Postal | 930037398 |
| Manufacturer Phone | 8056503391 |
| Manufacturer G1 | TMJ SOLUTIONS, INC. |
| Manufacturer Street | 6059 KING DRIVE |
| Manufacturer City | VENTURA CA 930037398 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 930037398 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PATIENT-FITTED TMJ RECONSTRUCTION PROSTHESIS |
| Generic Name | TEMPOROMANDIBULAR JOINT IMPLANT |
| Product Code | LZD |
| Date Received | 2020-01-21 |
| Model Number | TYY-NNNNM |
| Catalog Number | TYY-NNNNM |
| Lot Number | W45504 |
| Device Expiration Date | 2020-03-01 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TMJ SOLUTIONS, INC. |
| Manufacturer Address | 6059 KING DRIVE VENTURA CA 930037398 US 930037398 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2020-01-21 |