DONJOY TITANIUM, A22 CONV TITANIUM

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 2019-09-20 for DONJOY TITANIUM, A22 CONV TITANIUM manufactured by Djo, Llc.

MAUDE Entry Details

Report Number3012446970-2019-00033
MDR Report Key9100749
Report SourceCONSUMER
Date Received2019-09-20
Date of Report2019-09-20
Date of Event2019-08-20
Date Mfgr Received2019-08-28
Device Manufacturer Date2018-12-21
Date Added to Maude2019-09-20
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 ContactMR. BRIAN BECKER
Manufacturer Street2900 LAKE VISTA DRIVE
Manufacturer CityLEWISVILLE TX 75067
Manufacturer CountryUS
Manufacturer Postal75067
Manufacturer G1DJO, LLC
Manufacturer Street3151 SCOTT ST.
Manufacturer CityVISTA CA 920819663
Manufacturer CountryUS
Manufacturer Postal Code920819663
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDONJOY TITANIUM, A22
Generic NameJOINT, KNEE, EXTERNAL BRACE
Product CodeITQ
Date Received2019-09-20
Model NumberCONV TITANIUM
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDJO, LLC
Manufacturer Address1430 DECISION STREET VISTA CA 920819663 US 920819663


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2019-09-20

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