CHATTANOOGA 2090K

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2015-08-05 for CHATTANOOGA 2090K manufactured by Djo, Llc.

Event Text Entries

[22863282] Complaint received that alleges "customer sustained a broken leg while getting treatment. " product not returned for evaluation or review. No additional information received from patient or clinician regarding additional details of incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616086-2015-00019
MDR Report Key4995138
Report SourceUSER FACILITY
Date Received2015-08-05
Date of Report2015-07-29
Date of Event2015-07-10
Date Mfgr Received2015-07-10
Date Added to Maude2015-08-12
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 ContactMR WILLIAM FISHER
Manufacturer Street1430 DECISION ST.
Manufacturer CityVISTA CA 92081
Manufacturer CountryUS
Manufacturer Postal92081
Manufacturer Phone7607343126
Manufacturer G1DJ ORTHOPEDICS DE MEXICO, S.A. DE C.V.
Manufacturer StreetCARRETERA LIBRE TIJUANA TECATE 20230 SUBMETROPOLI EL FLORIDO
Manufacturer CityTIJUANA BAJA CALIFORNIA 22244
Manufacturer CountryMX
Manufacturer Postal Code22244
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCHATTANOOGA
Generic NameCPM
Product CodeBXB
Date Received2015-08-05
Model Number2090K
Catalog Number2090K
Lot Number19726
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDJO, LLC
Manufacturer Address1430 DECISION ST. VISTA CA 92081 US 92081


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2015-08-05

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