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 |