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 07 report with the FDA on 2005-11-21 for OFFSET ADAPTER 6478-6-490 manufactured by Stryker Orthopaedics Limerick.

Event Text Entries

[20509906] It was reported that the offset adapter had fractured.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610726-2005-00063
MDR Report Key652271
Report Source07
Date Received2005-11-21
Date of Report2005-11-03
Date of Event2005-10-31
Date Mfgr Received2005-11-03
Date Added to Maude2005-12-15
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 INTORRELLA
Manufacturer Street325 CORPORATE DRIVE
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 Received2005-11-21
Model NumberNA
Catalog Number6478-6-490
Lot Number7912574
ID NumberNI
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key641738
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 2005-11-21

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