MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2005-12-01 for * UNK manufactured by Unk.
[407087]
Pt complains of being exposed to electromagnetic device. Pt is being stalked by 2 men and they are playing seductive game with her. Pt was invited to participate in the game which is against the law. Fda needs to investigate.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1037349 |
| MDR Report Key | 650761 |
| Date Received | 2005-12-01 |
| Date of Report | 2005-12-01 |
| Date Added to Maude | 2005-12-12 |
| 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 | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | * |
| Generic Name | ELECTROMAGNETIC DEVICE |
| Product Code | GZI |
| Date Received | 2005-12-01 |
| Model Number | UNK |
| Catalog Number | UNK |
| Lot Number | UNK |
| ID Number | * |
| Operator | LAY USER/PATIENT |
| Device Availability | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 640234 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Life Threatening; 2. Required No Informationntervention | 2005-12-01 |