MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1999-03-24 for LAX-OPTICS UNK manufactured by Unk.
[19494899]
Pin hole glasses called lax-optics from another country are a fraud and all endorsements are lies and not true. Rptr suggests that the fda should apprehend all persons involved in fraud and endangering lives. Pin hole glasses are being sold in the usa.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1015976 |
| MDR Report Key | 215926 |
| Date Received | 1999-03-24 |
| Date of Report | 1999-03-24 |
| Date Added to Maude | 1999-03-29 |
| 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 |
| 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 | LAX-OPTICS |
| Generic Name | SPECIALIZED GLASSES |
| Product Code | HQZ |
| Date Received | 1999-03-24 |
| Model Number | UNK |
| Catalog Number | UNK |
| Lot Number | UNK |
| ID Number | UNK |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 209458 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 1999-03-24 |