PROFEMUR? MODULAR FEMORAL NECK PHA01202

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other report with the FDA on 2020-03-04 for PROFEMUR? MODULAR FEMORAL NECK PHA01202 manufactured by Microport Orthopedics Inc..

Event Text Entries

[182524482] Allegedly, patient was revised due to poly wear+pain without loosening components not revised: tige "anca fit? " rev. Hap 1/3 proximal 17. 5d, ppr67628, lot r0797645. 1.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010536692-2020-00188
MDR Report Key9788874
Report SourceFOREIGN,OTHER
Date Received2020-03-04
Date of Report2020-03-04
Date Facility Aware2019-07-02
Date Added to Maude2020-03-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
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 NamePROFEMUR? MODULAR FEMORAL NECK
Generic NameHIP COMPONENT
Product CodeLWJ
Date Received2020-03-04
Model NumberPHA01202
Catalog NumberPHA01202
Lot NumberV08215418
OperatorHEALTH PROFESSIONAL
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 2020-03-04

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