MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-19 for VERICHIP MICRO TRANSPONDER manufactured by Jamm Technologies.
[131310234]
I severed my spinal cord in 2007 and have been to 2 different hospitals since for care. I have a verichip or other brand of medical info micro transponder that has been hacked into and causing serious auditory and other stress related health problems. I cant get anyone at either hospital to admit that it's there or even respond to any correspondence.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5082372 |
| MDR Report Key | 8186454 |
| Date Received | 2018-12-19 |
| Date of Report | 2018-12-18 |
| Date of Event | 2017-11-01 |
| Date Added to Maude | 2018-12-20 |
| 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 | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | VERICHIP MICRO TRANSPONDER |
| Generic Name | IMPLANTABLE RADIOFREQUENCY TRANSPONDER SYSTEM |
| Product Code | NRV |
| Date Received | 2018-12-19 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | JAMM TECHNOLOGIES |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Life Threatening; 3. Other; 4. Deathisabilit | 2018-12-19 |