PLUS

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 2012-09-28 for PLUS manufactured by Smith&nephew -switzerland.

Event Text Entries

[2907434] It was reported that a revision surgery was performed due to dislocation. Prior to the revision surgery, the patient sustained a bone fracture under the stem and fixation with a plate was performed. The surgeon thinks that ante-version angle of stem was shifted by the bone fracture and the shifted angle was cause of this dislocation.
Patient Sequence No: 1, Text Type: D, B5


[10135538] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9613369-2012-00082
MDR Report Key2763735
Report Source07
Date Received2012-09-28
Date of Report2012-09-19
Date of Event2012-09-19
Date Mfgr Received2012-09-19
Date Added to Maude2012-09-28
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 FDA0
Event Location0
Manufacturer ContactMR PHILLIP EMMERT
Manufacturer Street1450 E. BROOKS RD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013995296
Manufacturer G1SMITH&NEPHEW - SWITZERLAND
Manufacturer StreetSCHACHENALLEE 29
Manufacturer CityAARAU CH5000
Manufacturer CountrySZ
Manufacturer Postal CodeCH5000
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePLUS
Generic NameFEMORAL COMPONENT
Product CodeLPF
Date Received2012-09-28
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSMITH&NEPHEW -SWITZERLAND
Manufacturer AddressSCHACHENALLEE 29 AARAU CH5000 SZ CH5000


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2012-09-28

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