UNKNOWN NEXGEN ROTATING HINGE KNEE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,08 report with the FDA on 2009-12-16 for UNKNOWN NEXGEN ROTATING HINGE KNEE manufactured by Zimmer, Inc..

Event Text Entries

[1256443] It is reported the devices were implanted in 2004, and the patient was revised in 2009, due to subluxation, painful joint block and dislocation of stud. No indication of trauma.
Patient Sequence No: 1, Text Type: D, B5


[8343713] This report will be amended when our investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1822565-2009-01199
MDR Report Key1561182
Report Source01,05,08
Date Received2009-12-16
Date of Report2009-11-16
Date of Event2009-10-23
Date Mfgr Received2009-11-23
Date Added to Maude2009-12-18
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 FDA0
Event Location0
Manufacturer ContactBRIAN FIEDLER
Manufacturer StreetP.O BOX 708
Manufacturer CityWARSAW IN 465810708
Manufacturer CountryUS
Manufacturer Postal465810708
Manufacturer Phone8006136131
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameUNKNOWN NEXGEN ROTATING HINGE KNEE
Generic NameKNEE PROSTHESIS
Product CodeHRZ
Date Received2009-12-16
Model NumberNA
Catalog NumberUNK
Lot NumberUNK
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerZIMMER, INC.
Manufacturer AddressP.O. BOX 708 WARSAW IN 46581070 US 46581 0708


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2009-12-16

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