MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2008-09-22 for RFID HUMAN IMPLANTABLE MICRO CHIP manufactured by Verichip.
[17069503]
Pt reports that she wants the micro chip removed, and cannot find anyone to remove the chip. Pt reports that she has done research and found that the chip causes cancer in animals.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5008348 |
| MDR Report Key | 1167299 |
| Date Received | 2008-09-22 |
| Date of Report | 2008-09-22 |
| Date of Event | 2008-07-01 |
| Date Added to Maude | 2008-09-26 |
| 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 | RFID HUMAN IMPLANTABLE MICRO CHIP |
| Generic Name | NONE |
| Product Code | NRV |
| Date Received | 2008-09-22 |
| Operator | LAY USER/PATIENT |
| Implant Flag | Y |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 1201177 |
| Manufacturer | VERICHIP |
| Manufacturer Address | DEL REY BEACH FL US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2008-09-22 |