REBOUND AIR WALKER B-242900003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2015-11-23 for REBOUND AIR WALKER B-242900003 manufactured by Ossur Americas.

Event Text Entries

[31914158]
Patient Sequence No: 1, Text Type: N, H10


[31914162] Patient using a rebound air walker walking boot claims the strap broke causing a fall. The pharmacy stated the patient claims they required a hospital visit, but is unable to verify.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2085446-2015-00002
MDR Report Key5243254
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2015-11-23
Date of Report2015-11-20
Date of Event2015-08-18
Date Mfgr Received2015-08-18
Date Added to Maude2015-11-23
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. KAREN MONTES
Manufacturer Street27051 TOWNE CENTRE DRIVE
Manufacturer CityFOOTHILL RANCH CA 92610
Manufacturer CountryUS
Manufacturer Postal92610
Manufacturer Phone9493823741
Manufacturer G1OSSUR AMERICAS
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
Generic NameJOINT, ANKLE, EXTERNAL BRACE
Product CodeITW
Date Received2015-11-23
Model NumberB-242900003
Catalog NumberB-242900003
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOSSUR AMERICAS
Manufacturer Address27051 TOWNE CENTRE FOOTHILL RANCH CA 92610 US 92610


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-11-23

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