LIFESTYLES SKIN 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 2015-04-29 for LIFESTYLES SKIN 7312 manufactured by Suretex Ltd..

Event Text Entries

[5827921] The customer informed ansell healthcare products, llc that after using a (b)(6)polyisoprene lubricated condom, his partner developed burning that required medical attention.
Patient Sequence No: 1, Text Type: D, B5


[13139748] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1019632-2015-00005
MDR Report Key4741908
Report Source04
Date Received2015-04-29
Date of Report2015-04-29
Date Facility Aware2015-04-28
Report Date2015-04-29
Date Reported to FDA2015-04-29
Date Reported to Mfgr2015-04-29
Date Mfgr Received2015-04-29
Device Manufacturer Date2014-08-01
Date Added to Maude2015-05-04
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 JIGANI-2ND PHASE
Manufacturer CityANEKAI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIFESTYLES SKIN
Generic NameLUBRICATED POLYISOPRENE CONDOM
Product CodeMOL
Date Received2015-04-29
Catalog Number7312
Lot Number1408P20722
Device Expiration Date2019-07-31
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Age2 YR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSURETEX LTD.
Manufacturer AddressBANGALORE IN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-04-29

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