BAND AID BRAND KPP BANDAGES 4901730080156

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign report with the FDA on 2020-03-30 for BAND AID BRAND KPP BANDAGES 4901730080156 manufactured by Johnson & Johnson Consumer Inc.

MAUDE Entry Details

Report Number2214133-2020-00014
MDR Report Key9900573
Report SourceCONSUMER,FOREIGN
Date Received2020-03-30
Date of Report2020-03-05
Date Mfgr Received2020-03-05
Date Added to Maude2020-03-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactLAURIE RAUCO
Manufacturer Street199 GRANDVIEW RD
Manufacturer CitySKILLMAN NJ 085589418
Manufacturer CountryUS
Manufacturer Postal085589418
Manufacturer Phone2152734905
Manufacturer G1COLOPLAST
Manufacturer StreetCOLOPLAST HUNGARY KFT. H-4300 HYIRBATOR
Manufacturer CityCOLOPLAST U.2
Manufacturer CountryHU
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBAND AID BRAND KPP BANDAGES
Generic NameDRESSING, WOUND, OCCLUSIVE
Product CodeNAD
Date Received2020-03-30
Model Number4901730080156
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerJOHNSON & JOHNSON CONSUMER INC
Manufacturer Address199 GRANDVIEW RD SKILLMAN NJ 085589418 US 085589418


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-30

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