FEMORAL HEAD 2600002X

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-01-02 for FEMORAL HEAD 2600002X manufactured by Microport Orthopedics Inc..

Event Text Entries

[173703795] This event will be updated once the investigation is complete. Trends will be evaluated.
Patient Sequence No: 1, Text Type: N, H10


[173703796] Allegedly, head and liner exchange, metal liner coming out and cocr head being revised 32mm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010536692-2020-00011
MDR Report Key9540429
Report SourceDISTRIBUTOR
Date Received2020-01-02
Date of Report2020-01-02
Date Facility Aware2019-12-06
Date Mfgr Received2019-12-06
Date Added to Maude2020-01-02
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 Street5677 AIRLINE ROAD
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal38002
Manufacturer Phone9018674771
Manufacturer G1MICROPORT ORTHOPEDICS INC.
Manufacturer Street5677 AIRLINE RD.
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal Code38002
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFEMORAL HEAD
Generic NameHIP COMPONENT
Product CodeJDL
Date Received2020-01-02
Model Number2600002X
Catalog Number2600002X
Lot NumberNI
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMICROPORT ORTHOPEDICS INC.
Manufacturer Address5677 AIRLINE RD. ARLINGTON TN 38002 US 38002


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-02

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