SKIN PREP NON STING WIPES 59420600

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 2016-08-19 for SKIN PREP NON STING WIPES 59420600 manufactured by Smith & Nephew Medical Ltd..

Event Text Entries

[52489901]
Patient Sequence No: 1, Text Type: N, H10


[52489902] It was reported that after using a skin prep wipe, a patient's catheter came out. This led to the patient wetting the bed and skin breakdown.
Patient Sequence No: 1, Text Type: D, B5


[79270257]
Patient Sequence No: 1, Text Type: N, H10


[107028399] [(b)(4)].
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8043484-2016-00106
MDR Report Key5888285
Report SourceCONSUMER
Date Received2016-08-19
Date of Report2018-03-22
Date Mfgr Received2016-08-04
Date Added to Maude2016-08-19
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 ContactMRS CLAUDIA ODOY
Manufacturer StreetSCHACHENALLEE 29
Manufacturer CityAARAU 5001
Manufacturer CountrySZ
Manufacturer Postal5001
Manufacturer Phone0628320660
Manufacturer G1SMITH & NEPHEW MEDICAL LTD.
Manufacturer Street101 HESSLE ROAD SUITE 126
Manufacturer CityHULL TX HU3 2BN
Manufacturer CountryUK
Manufacturer Postal CodeHU3 2BN
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSKIN PREP NON STING WIPES
Generic NameBANDAGE, LIQUID
Product CodeKMF
Date Received2016-08-19
Model Number59420600
Catalog Number59420600
Lot Number91290
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW MEDICAL LTD.
Manufacturer Address101 HESSLE ROAD HULL HU3 2BN UK HU3 2BN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-08-19

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