MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2006-12-15 for THE ZAPPER * manufactured by *.
[21697779]
I'm not sure if anything bad is going to happen, but i went into a chiropracter's office in order to get back adjusted and he hooked me up to a machine called "the zapper. " i have never been into a chiropracter before so i had no idea why i was being hooked up to this machine. He said it was supposed to eliminate all the "parasites" out of my body. Anyway, i felt nothing and thought it was completely crap. Now, i feel completely out of it and kind of dizzy. I'm not sure what that machine does, but i don't think it's good.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1041381 |
| MDR Report Key | 795319 |
| Date Received | 2006-12-15 |
| Date of Report | 2006-12-15 |
| Date of Event | 2006-12-15 |
| Date Added to Maude | 2006-12-19 |
| 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 | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | THE ZAPPER |
| Generic Name | * |
| Product Code | HCC |
| Date Received | 2006-12-15 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | N |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 782908 |
| Manufacturer | * |
| Manufacturer Address | * * * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2006-12-15 |