MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2005-02-02 for RIFE RESEARCH * manufactured by *.
[18330030]
Complainant purchased for $350. 00 a programmable frequency generator (pfg) model pfg-100 that had claims to heal or reverse disease processes. Complainant also provided a one page document titled "rife research laboratory" advertisting engineer and machinist and inventor of this machine, and offering to purchase from rockwell scientific research l. L. C. Complainant details in note of an individual that unsuccessfully used the pfg to treat prostrate cancer. Complainant alleges attempting break-ins to home where attempts were made to remove the literature and equipment. Complainant fears and wants confidentiality.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW4003860 |
| MDR Report Key | 570656 |
| Date Received | 2005-02-02 |
| Date of Report | 2004-12-21 |
| Date Added to Maude | 2005-02-08 |
| 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 | RIFE RESEARCH |
| Generic Name | PROGRAMMABLE FREQUENCY GENERATOR (PFG) |
| Product Code | GZI |
| Date Received | 2005-02-02 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 560503 |
| Manufacturer | * |
| Manufacturer Address | * * * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2005-02-02 |