SCULPSURE 100-7026-010

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 2016-11-09 for SCULPSURE 100-7026-010 manufactured by Cynosure Inc.

Event Text Entries

[59554146] Patient was prescribed an oral antibiotic as well as bacitracin ointment for intervention use for post treatment care. Treatment settings were within clinical guidelines. Device was evaluated and found to be operating as intended. Blisters are expected side effects from laser treatments, but reportable in this incident since the patient had medication for intervention use.
Patient Sequence No: 1, Text Type: N, H10


[59554147] Patient developed a large blister on the flanks from a laser procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1222993-2016-00055
MDR Report Key6090519
Report SourceCONSUMER
Date Received2016-11-09
Date of Report2016-11-09
Date of Event2016-09-27
Date Mfgr Received2016-10-14
Date Added to Maude2016-11-09
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 ContactCYNOSURE INC
Manufacturer Street5 CARLISLE RD.
Manufacturer CityWESTFORD MA 01886
Manufacturer CountryUS
Manufacturer Postal01886
Manufacturer Phone9783678736
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSCULPSURE
Generic NameSCULPSURE
Product CodePKT
Date Received2016-11-09
Catalog Number100-7026-010
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCYNOSURE INC
Manufacturer Address5 CARLISLE RD WESTFORD MA 01886 US 01886


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-11-09

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