REBOUND AIR WALKER MD B-242900003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2018-04-24 for REBOUND AIR WALKER MD B-242900003 manufactured by Ossur Americas, Inc..

Event Text Entries

[106330897] Patient claim of pressure and swelling on tendons while wearing orthopedic walking boot.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2085446-2018-00001
MDR Report Key7455123
Report SourceDISTRIBUTOR
Date Received2018-04-24
Date of Report2018-04-24
Date Mfgr Received2018-03-27
Date Added to Maude2018-04-24
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. CRYSTAL SWAFFORD
Manufacturer Street27051 TOWNE CENTRE
Manufacturer CityFOOTHILL RANCH CA 92610
Manufacturer CountryUS
Manufacturer Postal92610
Manufacturer Phone9493823817
Manufacturer G1OSSUR AMERICAS, INC.
Manufacturer Street27051 TOWNE CENTRE
Manufacturer CityFOOTHILL RANCH CA 92610
Manufacturer CountryUS
Manufacturer Postal Code92610
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameREBOUND AIR WALKER MD
Generic NameJOINT, ANKLE, EXTERNAL BRACE
Product CodeITW
Date Received2018-04-24
Returned To Mfg2018-03-27
Model NumberB-242900003
Catalog NumberB-242900003
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerOSSUR AMERICAS, INC.
Manufacturer Address27051 TOWNE CENTRE FOOTHILL RANCH CA 92610 US 92610


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-04-24

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