DONJOY DEFIANCE III CONV DEFIANCE III

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-02-11 for DONJOY DEFIANCE III CONV DEFIANCE III manufactured by Djo, Llc.

Event Text Entries

[182180357] No device was returned for evaluation. If the device is received, a follow-up report will be submitted upon completion of product evaluation.
Patient Sequence No: 1, Text Type: N, H10


[182180358] It was reported that the patient "lost my balance and did one or two cartwheels and pop. I'm guessing my knee was hyperextended as i was cartwheeling and as the ski popped off so did my acl (anterior cruciate ligament). I waited a couple minutes to let the pain subside but the second i tried to click back into my ski i knew the acl was gone. I skied down on my left ski to the door of the first aid clinic at the base of the resort. " no further information is currently available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012446970-2020-00004
MDR Report Key9694714
Report SourceCONSUMER
Date Received2020-02-11
Date of Report2020-02-16
Date of Event2020-01-10
Date Mfgr Received2020-01-28
Device Manufacturer Date2012-02-24
Date Added to Maude2020-02-11
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 FDA0
Report to FDA3
Event Location3
Manufacturer ContactBRIAN BECKER
Manufacturer Street2900 LAKE VISTA DRIVE
Manufacturer CityLEWISVILLE, TX
Manufacturer CountryUS
Manufacturer G1DJO, LLC
Manufacturer Street3151 SCOTT ST.
Manufacturer CityVISTA, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDONJOY DEFIANCE III
Generic NameJOINT, KNEE, EXTERNAL BRACE
Product CodeITQ
Date Received2020-02-11
Returned To Mfg2020-02-14
Model NumberCONV DEFIANCE III
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDJO, LLC
Manufacturer Address1430 DECISION STREET VISTA, CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-11

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