MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2006-07-23 for DENTURES * manufactured by *.
[15606760]
Dentist provided me with dentures that don't fit, over billed me for a visit and charged me for a procedure he did not perform. This was verified by other dentists. Put me at risk during an emergency visit, kept incomplete and inaccurate records. I went for over 15 months without eating one meal with dentures in. Many times opening sores in my mouth. I have two heart stents and a hip replacement. Dr. Refuses to provide me with the name of the lab that made them.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1039819 |
| MDR Report Key | 748981 |
| Date Received | 2006-07-23 |
| Date of Report | 2006-07-23 |
| Date of Event | 2004-12-09 |
| Date Added to Maude | 2006-08-16 |
| 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 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DENTURES |
| Generic Name | DENTURES |
| Product Code | NSL |
| Date Received | 2006-07-23 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 736762 |
| Manufacturer | * |
| Manufacturer Address | * * FL * US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2006-07-23 |