BAB FLEXIBLE FABRIC EXTRA LARGE 381370056850

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 2020-03-20 for BAB FLEXIBLE FABRIC EXTRA LARGE 381370056850 manufactured by Johnson & Johnson Consumer Inc.

MAUDE Entry Details

Report Number1000599868-2020-00003
MDR Report Key9861462
Report SourceCONSUMER
Date Received2020-03-20
Date of Report2020-02-26
Date of Event2020-02-26
Date Mfgr Received2020-02-26
Device Manufacturer Date2019-10-06
Date Added to Maude2020-03-20
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 ContactLAURIE RAUCO
Manufacturer Street199 GRANDVIEW RD
Manufacturer CitySKILLMAN NJ 085589418
Manufacturer CountryUS
Manufacturer Postal085589418
Manufacturer Phone2152734905
Manufacturer G1SHANGHAI JOHNSON & JOHNSON LTD
Manufacturer Street120 NAN YA ROAD
Manufacturer CityMINGHANG, SHANGHAI 200245
Manufacturer CountryCH
Manufacturer Postal Code200245
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBAB FLEXIBLE FABRIC EXTRA LARGE
Generic NameTAPE AND BANDAGE, ADHESIVE
Product CodeKGX
Date Received2020-03-20
Model Number381370056850
Lot Number191006
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 2020-03-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.