WIRE BAY PT CORTICAL 370MM 71102102

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 2013-02-27 for WIRE BAY PT CORTICAL 370MM 71102102 manufactured by Smith & Nephew, Inc..

Event Text Entries

[3171315] It was reported that a revision surgery was performed due to broken wires.
Patient Sequence No: 1, Text Type: D, B5


[10519761] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1020279-2013-00130
MDR Report Key2980948
Report Source07
Date Received2013-02-27
Date of Report2013-01-30
Date of Event2013-01-30
Date Mfgr Received2013-01-30
Device Manufacturer Date2012-04-01
Date Added to Maude2013-02-27
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 RD.
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 NameWIRE BAY PT CORTICAL 370MM
Generic NameCORTICAL WIRE
Product CodeDZK
Date Received2013-02-27
Catalog Number71102102
Lot Number12DM11799
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
101. Required No Informationntervention 2013-02-27

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