MBT REVISION CEM TIB TRAY SZ 4 1294-35-140 129435140

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-26 for MBT REVISION CEM TIB TRAY SZ 4 1294-35-140 129435140 manufactured by Depuy Orthopaedics Inc Us.

Event Text Entries

[188327172] (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


[188327173] The patient was revised to address proximal tibia fracture which caused the tray to collapse. The size 4 mbt rev tray, 29mm sleeve and 75 x 14 stem were removed and longer stem rev tray were placed. Doi: (b)(6) 2019. Dor: (b)(6) 2020; right knee.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2020-09383
MDR Report Key9884796
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-26
Date of Report2020-03-13
Date of Event2020-03-13
Date Mfgr Received2020-03-13
Device Manufacturer Date2019-07-03
Date Added to Maude2020-03-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. KARA DITTY-BOVARD
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone6107428552
Manufacturer G1JTE WARSAW MFG SITE
Manufacturer Street700 ORTHOPAEDIC DRIVE
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal Code465810988
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMBT REVISION CEM TIB TRAY SZ 4
Generic NameMBT TIBIAL TRAY : KNEE TIBIAL TRAY
Product CodeNJL
Date Received2020-03-26
Model Number1294-35-140
Catalog Number129435140
Lot NumberJ4133J
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
101. Required No Informationntervention 2020-03-26

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