SCULPSURE 100-7026-010 105-7026-000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2018-09-26 for SCULPSURE 100-7026-010 105-7026-000 manufactured by Cynosure Inc..

Event Text Entries

[121852717] In this incident, patient experienced a blister on the flanks area following a laser procedure with the sculpsure. User error was involved in this incident since it was also determined that the treatment was performed over stretchmarks. The clinical reference guide was not followed as it cautions: "never treat over open areas, rashes, healing wounds or any skin that is not intact. Document any stretch marks, scars, prominent vessels, moles, tattoos, or skin irregularities. " the patient sought medical intervention at urgent care. There was no medication prescribed to the patient in this event. The device was evaluated and found to be operating as intended within specification. Blisters are expected side effects from laser treatments, however this is reportable because the patient had medical intervention.
Patient Sequence No: 1, Text Type: N, H10


[121852718] Patient had medical intervention following a laser procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222993-2018-00021
MDR Report Key7911676
Report SourceCONSUMER
Date Received2018-09-26
Date of Report2018-09-26
Date of Event2018-08-26
Date Mfgr Received2018-08-28
Device Manufacturer Date2017-04-05
Date Added to Maude2018-09-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street5 CARLISLE ROAD
Manufacturer CityWESTFORD MA 01886
Manufacturer CountryUS
Manufacturer Postal01886
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSCULPSURE
Generic NameSCULPSURE
Product CodePKT
Date Received2018-09-26
Model Number100-7026-010
Catalog Number105-7026-000
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCYNOSURE INC.
Manufacturer Address5 CARLISLE ROAD WESTFORD MA 01886 US 01886


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-09-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.