MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-10-04 for EDITOR'S CHOICE * manufactured by Unk.
[330493]
There is no info or address on a reading glass that was purchased at a big lots store.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1029750 |
| MDR Report Key | 490066 |
| Date Received | 2003-10-04 |
| Date of Report | 2003-10-04 |
| Date of Event | 2003-10-02 |
| Date Added to Maude | 2003-10-22 |
| 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 | 0 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | EDITOR'S CHOICE |
| Generic Name | READING GLASSES |
| Product Code | HOI |
| Date Received | 2003-10-04 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 478810 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2003-10-04 |