LIFESTYLES SKYN 7312

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 2014-06-16 for LIFESTYLES SKYN 7312 manufactured by Suretex Ltd.

Event Text Entries

[4531640] The customer informed ansell healthcare products, llc that after using a lifestyles polyisoprene lubricated condom she suffered severe vaginal burning that required medical attention.
Patient Sequence No: 1, Text Type: D, B5


[12128073] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1019632-2014-00010
MDR Report Key3940727
Report Source04
Date Received2014-06-16
Date of Report2014-06-16
Date Facility Aware2014-06-16
Report Date2014-06-16
Date Reported to FDA2014-06-16
Date Reported to Mfgr2014-06-16
Date Mfgr Received2014-06-16
Device Manufacturer Date2013-10-01
Date Added to Maude2014-07-18
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
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 Street1635 INDUSTRIAL RD.
Manufacturer CityDOTHAN AL 36303
Manufacturer CountryUS
Manufacturer Postal36303
Manufacturer Phone3346152566
Manufacturer G1SURETEX LTD.
Manufacturer StreetPLOT NO. 74 TO 91 KIADB IND. ESTATE
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIFESTYLES SKYN
Generic NameLUBRICATED POLYISOPRENE CONDOM
Product CodeMOL
Date Received2014-06-16
Returned To Mfg2014-06-16
Catalog Number7312
Lot Number1310100622
Device Expiration Date2016-09-30
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Age1 YR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSURETEX LTD
Manufacturer AddressBANGALORE IN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2014-06-16

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