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 2015-04-17 for LIFESTYLES SKYN 7312 manufactured by Suretex Ltd..

Event Text Entries

[5584608] The customers boyfriend informed ansell (b)(6) that after using a lifestyles polyisoprene lubricated condom an epic pen was used and an ambulance called that took her to the hosp and she was given a further dose of medication to cure anaphylactic shock.
Patient Sequence No: 1, Text Type: D, B5


[13139182] (b)(4) - ansell healthcare products llc is submitting this report on behalf of suretex ltd. Incident occurred in the uk; however, the skyn product is also sold in the usa.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1019632-2015-00004
MDR Report Key4736145
Report Source04
Date Received2015-04-17
Date of Report2015-04-17
Date Facility Aware2014-07-28
Report Date2015-04-17
Date Reported to FDA2015-04-17
Device Manufacturer Date2013-05-01
Date Added to Maude2015-04-30
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 Location0
Manufacturer Street1635 INDUSTRIAL RD.
Manufacturer CityDOTHAN AL 36303
Manufacturer CountryUS
Manufacturer Postal36303
Manufacturer Phone3346152566
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIFESTYLES SKYN
Generic NameLUBRICATED POLYISOPRENE CONDOM
Product CodeMOL
Date Received2015-04-17
Catalog Number7312
Lot Number1305033016
Device Expiration Date2016-04-01
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Age1 YR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSURETEX LTD.
Manufacturer AddressSURAT THANI TH


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-04-17

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