KERRAFOAM? SIMPLE BORDER DRESSING

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-03-27 for KERRAFOAM? SIMPLE BORDER DRESSING manufactured by Crawford Healthcare Ltd.

MAUDE Entry Details

Report Number3004051837-2020-00004
MDR Report Key9892331
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2020-03-27
Date of Report2020-03-27
Date of Event2020-02-26
Date Mfgr Received2020-02-26
Date Added to Maude2020-03-27
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 ContactMR. ANDREW JACKSON
Manufacturer StreetKING EDWARD COURT KING EDWARD ROAD
Manufacturer CityKNUTSFORD, WA16 0BE, GBR
Manufacturer CountryUK
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKERRAFOAM? SIMPLE BORDER DRESSING
Generic NameOMP
Product CodeOMP
Date Received2020-03-27
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCRAWFORD HEALTHCARE LTD
Manufacturer AddressKING EDWARD COURT KING EDWARD ROAD KNUTSFORD, WA16 0BE UK


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-27

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