MOST OPTIONS HINGE KIT 502001001

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 2008-03-27 for MOST OPTIONS HINGE KIT 502001001 manufactured by Zimmer, Inc..

Event Text Entries

[20347308] It is reported that the axle is too large for the bushings.
Patient Sequence No: 1, Text Type: D, B5


[20551706] This report will be amended when our investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1822565-2008-00134
MDR Report Key1021549
Report Source05,08
Date Received2008-03-27
Date of Report2008-02-20
Date of Event2008-02-20
Date Facility Aware2008-02-20
Report Date2008-02-20
Date Mfgr Received2008-02-26
Device Manufacturer Date2007-10-01
Date Added to Maude2008-07-07
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 ContactANN RECKTENWALL
Manufacturer StreetP.O. BOX 708
Manufacturer CityWARSAW IN 465810708
Manufacturer CountryUS
Manufacturer Postal465810708
Manufacturer Phone5743718028
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameMOST OPTIONS HINGE KIT
Generic NameKNEE PROSTHESIS
Product CodeHRZ
Date Received2008-03-27
Returned To Mfg2008-02-26
Model NumberNA
Catalog Number502001001
Lot Number60812403
ID NumberNA
Device Expiration Date2012-09-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeNA
Device Eval'ed by MfgrN
Implant FlagY
Date RemovedB
Device Sequence No1
Device Event Key1020443
ManufacturerZIMMER, INC.
Manufacturer AddressP.O. BOX 708 WARSAW IN 465810708 US


Patients

Patient NumberTreatmentOutcomeDate
10 2008-03-27

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