STAYFREE ULTRA THIN MAXI WINGS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2011-01-03 for STAYFREE ULTRA THIN MAXI WINGS manufactured by Johnson & Johnson, Inc..

Event Text Entries

[1776355] Consumer placed product into underwear in anticipation of her menstruation, within a few mins, she began to experience a burning sensation. Product was discontinued, she saw her doctor who confirmed irritation and prescribed cortisone cream. The irritation worsened and the wound was described and required approx 18 stitches.
Patient Sequence No: 1, Text Type: D, B5


[8925474] Date of this submission is (b)(4) 2011. This closes out this report unless additional significant info is received.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8022269-2011-00001
MDR Report Key1956585
Report Source04
Date Received2011-01-03
Date of Report2010-12-05
Date of Event2010-12-03
Date Mfgr Received2010-12-05
Date Added to Maude2011-01-14
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 FDA0
Event Location0
Manufacturer ContactBRAD LAMOTTE
Manufacturer Street185 TABOR RD
Manufacturer CityMORRIS PLAINS NJ 07950
Manufacturer CountryUS
Manufacturer Postal07950
Manufacturer Phone9733853667
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTAYFREE ULTRA THIN MAXI WINGS
Generic NameNONE
Product CodeHHD
Date Received2011-01-03
Lot Number3169M6337
OperatorLAY USER/PATIENT
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerJOHNSON & JOHNSON, INC.
Manufacturer Address7101 RUE NOTRE-DAME E MONTREAL, QUEBEC


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2011-01-03

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