DYNASTY? BF SHELL 58MM GROUP G DSBFGG58

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 2020-01-10 for DYNASTY? BF SHELL 58MM GROUP G DSBFGG58 manufactured by Microport Orthopedics Inc..

Event Text Entries

[174686861] Allegedly, patient was revised on due to the patient dislocating. All components removed, replaced with different manufacturers system, apart from the 36mm mpo femoral head, which was removed and replaced with a 28mm mpo femoral head. (b)(6).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010536692-2020-00029
MDR Report Key9577049
Report SourceDISTRIBUTOR
Date Received2020-01-10
Date of Report2020-01-10
Date Facility Aware2019-10-15
Date Mfgr Received2019-10-15
Date Added to Maude2020-01-10
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 NameDYNASTY? BF SHELL 58MM GROUP G
Generic NameHIP COMPONENT
Product CodeJDL
Date Received2020-01-10
Model NumberDSBFGG58
Catalog NumberDSBFGG58
Lot Number1753057
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 2020-01-10

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