MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2017-06-28 for SCULPSURE 100-7026-010 manufactured by Cynosure Inc.
[78653250]
Patient was prescribed antibiotics to treat the affected area and had a incision/drainage procedure on the affected nodule. The device was evaluated and found to be operating as intended. Nodules are expected side effects from sculpsure laser treatments, but reportable in this incident since the patient had an intervention procedure.
Patient Sequence No: 1, Text Type: N, H10
[78653251]
Patient had medical intervention for a nodule on the flanks area.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1222993-2017-00029 |
| MDR Report Key | 6675172 |
| Report Source | CONSUMER |
| Date Received | 2017-06-28 |
| Date of Report | 2017-06-28 |
| Date of Event | 2017-04-20 |
| Date Mfgr Received | 2017-06-02 |
| Date Added to Maude | 2017-06-28 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Street | 5 CARLISLE RD |
| Manufacturer City | WESTFORD MA 01886 |
| Manufacturer Country | US |
| Manufacturer Postal | 01886 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SCULPSURE |
| Generic Name | SCULPSURE |
| Product Code | PKT |
| Date Received | 2017-06-28 |
| Catalog Number | 100-7026-010 |
| Device Availability | N |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CYNOSURE INC |
| Manufacturer Address | 5 CARLISLE RD WESTFORD MA 01886 US 01886 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-06-28 |