JET X 71051043

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2004-09-30 for JET X 71051043 manufactured by Smith & Nephew, Inc., Orthopaedic Div..

Event Text Entries

[328177] Revision surgery was performed due to the device broke.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1020279-2004-00580
MDR Report Key546910
Report Source05,07
Date Received2004-09-30
Date of Report2004-09-30
Date Mfgr Received2004-08-31
Device Manufacturer Date2002-12-01
Date Added to Maude2004-10-05
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 FDA3
Event Location3
Manufacturer ContactMR JASON CHAMNESS, SPECIALIST
Manufacturer Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013995899
Manufacturer G1SMITH & NEWPHEW 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 NameJET X
Generic NameLONG CENTRAL BODY
Product CodeJDD
Date Received2004-09-30
Returned To Mfg2004-08-31
Model NumberNA
Catalog Number71051043
Lot Number02MM02359
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeUNKNOWN
Device Eval'ed by MfgrN
Implant FlagY
Date RemovedU
Device Sequence No1
Device Event Key536318
ManufacturerSMITH & NEPHEW, INC., ORTHOPAEDIC DIV.
Manufacturer Address1450 E. BROOKS RD. MEMPHIS TN 38116 US
Baseline Brand NameJET X
Baseline Generic NameCENTRAL BODY
Baseline Model NoNA
Baseline Catalog No71051043
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2004-09-30

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