LEGION CON ART INS 9MM SZ 5-6 71420537

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 2014-10-03 for LEGION CON ART INS 9MM SZ 5-6 71420537 manufactured by Smith & Nephew, Inc..

Event Text Entries

[4933622] It was reported that a revision surgery was performed due to disassociation.
Patient Sequence No: 1, Text Type: D, B5


[12426717]
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1020279-2014-00613
MDR Report Key4140784
Report Source07
Date Received2014-10-03
Date of Report2014-10-03
Date of Event2014-10-03
Date Facility Aware2014-09-26
Date Mfgr Received2014-09-26
Device Manufacturer Date2012-02-01
Date Added to Maude2014-10-03
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. CONNIE MCBROOM
Manufacturer Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013995985
Manufacturer G1SMITH & NEPHEW, INC.
Manufacturer Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal Code38116
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLEGION CON ART INS 9MM SZ 5-6
Generic NameKNEE IMPLANT
Product CodeHSA
Date Received2014-10-03
Catalog Number71420537
Lot Number12BM78894
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address1450 BROOKS ROAD MEMPHIS TN 38116 US 38116


Patients

Patient NumberTreatmentOutcomeDate
10 2014-10-03

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