CHATTANOOGA HYDROCOLLATOR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2013-04-01 for CHATTANOOGA HYDROCOLLATOR manufactured by Djo, Llc.

Event Text Entries

[3412482] "received court documents stating that the plaintiff was electrocuted by a hydrocollator while attempting to unplug the product from an electrical outlet. " initial notification of complaint was a copy of court document notification of civil action. No additional info supplied to us for eval. Product not returned to us for eval.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616086-2013-00002
MDR Report Key3032496
Report Source99
Date Received2013-04-01
Date of Report2013-04-01
Date of Event2011-08-22
Date Mfgr Received2013-03-04
Date Added to Maude2013-04-04
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 G1DJ ORTHOPEDICS DE MEXICO, S.A. DE C.V.
Manufacturer Street20230 SUBMETROPOLI EL FLORIDO CARRETERA LIBRE TIJUANA TECATE
Manufacturer CityTIJUANA 22244
Manufacturer CountryMX
Manufacturer Postal Code22244
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCHATTANOOGA HYDROCOLLATOR
Generic NameHYDROCOLLATOR
Product CodeIMA
Date Received2013-04-01
Device AvailabilityN
Device AgeDA
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. Other 2013-04-01

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