TRI-LOCK TI 15.0 LAT OFFSET 101212150

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,other report with the FDA on 2020-03-16 for TRI-LOCK TI 15.0 LAT OFFSET 101212150 manufactured by Depuy Orthopaedics Inc Us.

Event Text Entries

[187029265] (b)(4). Initial reporter occupation: lawyer. (b)(4). If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[187029266] Pinnacle claim form and medical records received. After review of medical records, it was reported that the patient has elevated metal ion levels. There was no known revision details provided. Doi: (b)(6) 2007 - dor: none reported (left hip)
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2020-07935
MDR Report Key9834616
Report SourceCONSUMER,OTHER
Date Received2020-03-16
Date of Report2020-02-26
Date Mfgr Received2020-02-26
Device Manufacturer Date2007-03-09
Date Added to Maude2020-03-16
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKARA DITTY-BOVARD
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1DEPUY ORTHOPAEDICS, INC. 1818910
Manufacturer Street700 ORTHOPAEDIC DR.
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal Code465810988
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRI-LOCK TI 15.0 LAT OFFSET
Generic NameTRILOCK HIP STEM : HIP FEMORAL STEM
Product CodeKWL
Date Received2020-03-16
Catalog Number101212150
Lot NumberBH6C21000
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY ORTHOPAEDICS INC US
Manufacturer Address700 ORTHOPAEDIC DRIVE WARSAW IN 465810988 US 465810988


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-16

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