AIRCAST 01EP-L

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 2018-07-24 for AIRCAST 01EP-L manufactured by Djo, Llc.

Event Text Entries

[114845693] Complaint received that alleges "after short time of wearing the walker wounds the patients foot".
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616086-2018-00018
MDR Report Key7714381
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2018-07-24
Date of Report2018-12-19
Date of Event2018-07-12
Date Mfgr Received2018-07-12
Date Added to Maude2018-07-24
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 ContactBRIAN BECKER
Manufacturer Street1430 DECISION ST
Manufacturer CityVISTA CA 920819663
Manufacturer CountryUS
Manufacturer Postal920819663
Manufacturer Phone7607343126
Manufacturer G1DJO, LLC
Manufacturer Street1430 DECISION ST 20230 SUBMETROPOLI EL FLORIDO
Manufacturer CityVISTA CA 920819663
Manufacturer CountryUS
Manufacturer Postal Code920819663
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAIRCAST
Generic NameAIRSELECT, ELITE, LARGE
Product CodeITW
Date Received2018-07-24
Model Number01EP-L
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDJO, LLC
Manufacturer Address1430 DECISION ST VISTA CA 920819663 US 920819663


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-07-24

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