UNK J & J KNEE INSERT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,08 report with the FDA on 2005-05-31 for UNK J & J KNEE INSERT manufactured by Depuy Orthopaedics, Inc..

Event Text Entries

[398960] The pt was revised due to a fractured right femoral component. Poly wear was observed on the insert.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1818910-2005-00801
MDR Report Key608479
Report Source05,08
Date Received2005-05-31
Date of Report2005-05-17
Date of Event2005-05-17
Date Facility Aware2005-05-17
Report Date2005-05-17
Date Mfgr Received2005-05-17
Date Added to Maude2005-06-02
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 ContactGINNY STAMBERGER, MGR
Manufacturer Street700 ORTHOPAEDIC DR
Manufacturer CityWARSAW IN 465810988
Manufacturer CountryUS
Manufacturer Postal465810988
Manufacturer Phone5743727333
Manufacturer G1DEPUY ORTHOPAEDICS, INC
Manufacturer Street700 ORTHOPAEDIC DR
Manufacturer CityWARSAW IN 46581098
Manufacturer CountryUS
Manufacturer Postal Code46581 0988
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameUNK J & J KNEE INSERT
Generic NameTOTAL KNEE REPLACEMENT
Product CodeJHW
Date Received2005-05-31
Model NumberNA
Catalog NumberUNK
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age10 YR
Device Eval'ed by MfgrY
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key598276
ManufacturerDEPUY ORTHOPAEDICS, INC.
Manufacturer Address700 ORTHOPAEDIC DR. WARSAW IN 465810988 US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2005-05-31

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