FOOT ELEVATOR 6533

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 2019-06-13 for FOOT ELEVATOR 6533 manufactured by Posey Products Llc.

MAUDE Entry Details

Report Number2020362-2019-00149
MDR Report Key8696740
Report SourceCONSUMER
Date Received2019-06-13
Date of Report2019-05-15
Date Mfgr Received2019-05-15
Date Added to Maude2019-06-13
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 ContactWILLIAM HINCY
Manufacturer Street5635 PECK ROAD
Manufacturer CityARCADIA CA 91006
Manufacturer CountryUS
Manufacturer Postal91006
Manufacturer Phone6264433143
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFOOT ELEVATOR
Generic NamePROTECTOR, SKIN PRESSURE
Product CodeFMP
Date Received2019-06-13
Model Number6533
Catalog Number6533
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerPOSEY PRODUCTS LLC
Manufacturer Address5635 PECK ROAD ARCADIA CA 91006 US 91006


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-06-13

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