MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-02-17 for RIFE MACHINE manufactured by .
[19579913]
I have been hearing an interfering signal on my amateur radio equipment. I have tracked this down to what appears to be a rife machine in my neighborhood. I am in process of finding the location of the device and hope to have a house number to provided in the near future. I have been giving info on this to (b)(6) at the (b)(6) as i have found it.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5031525 |
| MDR Report Key | 3305273 |
| Date Received | 2013-02-17 |
| Date of Report | 2013-02-17 |
| Date Added to Maude | 2013-08-26 |
| 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 | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | RIFE MACHINE |
| Generic Name | NONE |
| Product Code | LDQ |
| Date Received | 2013-02-17 |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-02-17 |