12.5MM ENTRY REAMER 71631116

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2019-12-02 for 12.5MM ENTRY REAMER 71631116 manufactured by Smith & Nephew, Inc..

Event Text Entries

[177163286] It was reported that during surgery after reaming while removing the device was broken; the gray part and the silver metal part split. No harm to patient. No delay. No backup device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1020279-2019-04222
MDR Report Key9395915
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2019-12-02
Date of Report2020-02-20
Date of Event2019-11-05
Date Mfgr Received2020-02-14
Device Manufacturer Date2016-09-13
Date Added to Maude2019-12-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactDR SARAH FREESTONE
Manufacturer StreetSMITH & NEPHEW, INC. 1450 BROOKS ROAD
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 Name12.5MM ENTRY REAMER
Generic NameSYSTEM, ANALYSIS, ELECTRPHOETIC HEMOGLOBIN
Product CodeJBD
Date Received2019-12-02
Returned To Mfg2020-01-28
Catalog Number71631116
Lot Number16JM04782
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address1450 BROOKS ROAD MEMPHIS TN 38116 US 38116


Patients

Patient NumberTreatmentOutcomeDate
10 2019-12-02

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