CHATTANOOGA 2760

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2015-01-14 for CHATTANOOGA 2760 manufactured by Djo.

Event Text Entries

[5417675] Complaint received from clinician that alleges "pt received 3rd degree burns". Questionnaire was received from clinician and/or pt. Pt received 2nd degree burn under one pad and a 3rd degree burn under one pad. Pt was seen by his doctor and a burn specialist for diagnosis and treatment, no description of treatment revealed to mfr. Device not returned to mfr for evaluation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616086-2015-00001
MDR Report Key4420614
Report Source06
Date Received2015-01-14
Date of Report2015-01-13
Date of Event2014-12-18
Date Added to Maude2015-01-16
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 FDA3
Report to FDA0
Event Location0
Manufacturer Street1430 DECISION ST
Manufacturer CityVISTA CA 92081
Manufacturer CountryUS
Manufacturer Postal92081
Manufacturer Phone7607271280
Manufacturer G1DJ ORTHOPEDICS DE MEXICO, S.A. DE C.V.
Manufacturer StreetCARRETERA LIBRE TIJUANA TECATE 20230 SUBMETROPOLI EL FLORIDO
Manufacturer CityTIJUANA B.C. 22244
Manufacturer CountryMX
Manufacturer Postal Code22244
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCHATTANOOGA
Generic NameINTELECT LEGEND XT COMBOUS STD
Product CodeGZI
Date Received2015-01-14
Model Number2760
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDJO
Manufacturer Address1430 DECOISION ST VISTA CA 92081 US 92081


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-01-14

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