INTELLECT MOBILE COMBO 2778

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2011-09-22 for INTELLECT MOBILE COMBO 2778 manufactured by Dj Orthopedics De Mexico.

Event Text Entries

[2159024] Event was reported from an international (hk) clinician that he observed what was identified as burns or scarring in the treatment area of a patient during a follow up visit. The clinician indicated there was no need to interrupt therapy or provide medical intervention. The clinical facility possesses three (3) cat. # 2778 intelect mobile combo devices, but could not be certain which device the therapy was provided. The device has not yet been received by djo for evaluation but it could be reasonably assumed that the device may have contributed to the adverse event.
Patient Sequence No: 1, Text Type: D, B5


[9349011] Device has not been received from clinician as of (b)(4) 2011 (b)(4) supplemental report, if relevant data becomes available, will be submitted to fda.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9616086-2011-00118
MDR Report Key2265488
Report Source05
Date Received2011-09-22
Date of Report2011-09-22
Date of Event2011-08-23
Date Mfgr Received2011-06-23
Date Added to Maude2011-09-28
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 FDA0
Event Location0
Manufacturer Street1430 DECISION STREET
Manufacturer CityVISTA CA 92081
Manufacturer CountryUS
Manufacturer Postal92081
Manufacturer Phone7607343047
Manufacturer G1DJ ORTHOPEDICS DE MEXICO
Manufacturer CityTIJUANA B.C. 22244
Manufacturer CountryMX
Manufacturer Postal Code22244
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINTELLECT MOBILE COMBO
Generic NameELECTROTHERAPY
Product CodeIMG
Date Received2011-09-22
Model Number2778
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDJ ORTHOPEDICS DE MEXICO
Manufacturer AddressTIJUANA B.C. 22244 MX 22244


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2011-09-22

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