OXINIUM FEM HD 12/14 32MM +4 71343204

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-01-10 for OXINIUM FEM HD 12/14 32MM +4 71343204 manufactured by Smith & Nephew, Inc..

Event Text Entries

[132591437]
Patient Sequence No: 1, Text Type: N, H10


[132591438] Revision surgery was performed due to postoperative bone fracture.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1020279-2019-00102
MDR Report Key8233305
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-01-10
Date of Report2019-03-21
Date of Event2018-12-10
Date Mfgr Received2018-12-17
Date Added to Maude2019-01-10
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 ContactDR SARAH FREESTONE
Manufacturer Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone0447940038
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 NameOXINIUM FEM HD 12/14 32MM +4
Generic NameABSORBER, CARBON-DIOXIDE
Product CodeBSF
Date Received2019-01-10
Catalog Number71343204
Lot Number18HM00686
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address1450 BROOKS ROAD MEMPHIS TN 38116 US 38116


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-01-10

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