OFFSET ADAPTER 6478-6-490

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,01 report with the FDA on 2007-03-07 for OFFSET ADAPTER 6478-6-490 manufactured by Stryker Orthopaedics Limerick.

Event Text Entries

[587432] It was reported that the pt had to undergo a revision as the offset bolt had snapped at the hinge.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610726-2007-00008
MDR Report Key824956
Report Source00,01
Date Received2007-03-07
Date of Report2006-11-16
Date of Event2006-10-30
Date Mfgr Received2007-02-07
Date Added to Maude2007-03-12
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 Location0
Manufacturer ContactRITA INTORRELA
Manufacturer Street325 CORPORATE DR
Manufacturer CityMAHWAH NJ 07430
Manufacturer CountryUS
Manufacturer Postal07430
Manufacturer Phone2018315000
Manufacturer G1STRYKER ORTHOPAEDICS LIMERICK
Manufacturer StreetRAHEEN BUSINESS PARK
Manufacturer CityLIMERICK
Manufacturer CountryEI
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameOFFSET ADAPTER
Generic NameIMPLANT
Product CodeFJP
Date Received2007-03-07
Model NumberNA
Catalog Number6478-6-490
Lot NumberMAR199A
ID NumberNI
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key812356
ManufacturerSTRYKER ORTHOPAEDICS LIMERICK
Manufacturer Address* LIMERICK EI
Baseline Brand NameOFFSET ADAPTER
Baseline Generic NameIMPLANT
Baseline Model NoNA
Baseline Catalog No6478-6-490
Baseline IDNI


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2007-03-07

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