PROFORM HIP SYSTEM SC2677-40

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2017-12-19 for PROFORM HIP SYSTEM SC2677-40 manufactured by Stelkast Inc..

Event Text Entries

[95636474] An evaluation of the device cannot be performed as the device was not returned.
Patient Sequence No: 1, Text Type: N, H10


[95636475] During a left hip surgery, a 6. 5 x 40mm cancellous bone screw broke while being implanted. Only the head of the screw was retrieved. The distal third of the screw remains in the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2530191-2017-00173
MDR Report Key7128542
Report SourceCOMPANY REPRESENTATIVE
Date Received2017-12-19
Date of Report2017-12-19
Date of Event2017-12-08
Date Mfgr Received2017-12-08
Device Manufacturer Date2015-02-02
Date Added to Maude2017-12-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JOHN REYHER
Manufacturer Street200 HIDDEN VALLEY ROAD
Manufacturer CityMCMURRAY PA 15317
Manufacturer CountryUS
Manufacturer Postal15317
Manufacturer Phone7249416368
Manufacturer G1STELKAST INC.
Manufacturer Street200 HIDDEN VALLEY ROAD
Manufacturer CityMCMURRAY PA 15317
Manufacturer CountryUS
Manufacturer Postal Code15317
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROFORM HIP SYSTEM
Generic Name6.5MM CANCELLOUS BONE SCREW
Product CodeJDO
Date Received2017-12-19
Model NumberSC2677-40
Lot Number33173250202
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTELKAST INC.
Manufacturer Address200 HIDDEN VALLEY ROAD MCMURRAY PA 15317 US 15317


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2017-12-19

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