EXOGEN 4000 71034100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2012-03-21 for EXOGEN 4000 71034100 manufactured by Smith & Nephew Orthopaedics, Inc..

Event Text Entries

[2629736] It was reported that a patient developed skin sores while using the exogen unit.
Patient Sequence No: 1, Text Type: D, B5


[9761485] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1020279-2012-00178
MDR Report Key2498940
Report Source04
Date Received2012-03-21
Date of Report2012-03-20
Date of Event2012-03-20
Date Mfgr Received2012-03-20
Device Manufacturer Date2012-01-01
Date Added to Maude2012-03-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
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 AND NEPHEW, INC.
Manufacturer Street1450E. BROOKS RD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal Code38116
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEXOGEN 4000
Generic NameBONE GROWTH STIMULATOR
Product CodeLPQ
Date Received2012-03-21
Catalog Number71034100
Lot Number0112003927E
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW ORTHOPAEDICS, INC.
Manufacturer Address1450 BROOKS ROAD MEMPHIS TN 38116 US 38116


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2012-03-21

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