MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-01-22 for FASCIABLASTER manufactured by Adb Interests, Llc.
[98071786]
I had been using the fascia blaster as i was told per (b)(6). I was told that my cellulite wouldn't come back after using the fascia blaster, that bruising was good, go to a pain that was a level 7, and to blast on bruising caused by the fascia blaster as long as it didn't hurt. I had really bad bruising that never went away on the outside of both legs. I have what they call "staining" that is iron trapped below the skin.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5074718 |
| MDR Report Key | 7212004 |
| Date Received | 2018-01-22 |
| Date of Report | 2018-01-19 |
| Date of Event | 2016-06-09 |
| Date Added to Maude | 2018-01-23 |
| 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 | FASCIABLASTER |
| Generic Name | FASCIABLASTER |
| Product Code | IOD |
| Date Received | 2018-01-22 |
| Operator | LAY USER/PATIENT |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ADB INTERESTS, LLC |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-01-22 |