TC-PLUS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,01,07 report with the FDA on 2009-11-02 for TC-PLUS manufactured by Aarau Switzerland Manufacturing Site.

Event Text Entries

[1304975] It has been reported to smith & nephew that a revision surgery was performed due to loosening. The revision occurred approximately 1-3 years after implantation. This is all of the info that has been received at this time.
Patient Sequence No: 1, Text Type: D, B5


[8356787] Na
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9613369-2009-00160
MDR Report Key1520612
Report Source00,01,07
Date Received2009-11-02
Date of Report2009-11-02
Date Mfgr Received2009-10-02
Date Added to Maude2009-11-06
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 ContactMRS. LEAH EASLEY
Manufacturer Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013996137
Manufacturer G1AARAU SWITZERLAND MANUFACTURING SITE
Manufacturer StreetSCHACHENALLEE 29
Manufacturer CityAARAU 5000
Manufacturer CountrySZ
Manufacturer Postal Code5000
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameTC-PLUS
Generic NameFEMORAL/TIBIAL / KRP
Product CodeKRP
Date Received2009-11-02
Model NumberNA
Catalog NumberNI
Lot NumberNI
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAARAU SWITZERLAND MANUFACTURING SITE
Manufacturer AddressAARAU SZ


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2009-11-02

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