BHR 90127629

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2007-04-30 for BHR 90127629 manufactured by Smith & Nephew, Inc., Orthopaedic Div..

Event Text Entries

[19490386] It was reported revision surgery was performed due to femoral neck fracture.
Patient Sequence No: 1, Text Type: D, B5


[19736886] Na
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1020279-2007-00095
MDR Report Key844752
Report Source05
Date Received2007-04-30
Date of Report2007-04-26
Date of Event2006-10-18
Date Mfgr Received2007-04-26
Date Added to Maude2007-05-08
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 Location0
Manufacturer ContactMRS MELANIE TRAVIS
Manufacturer Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013996233
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 NameBHR
Generic NameCUP
Product CodeJDD
Date Received2007-04-30
Model NumberNA
Catalog Number90127629
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key831945
ManufacturerSMITH & NEPHEW, INC., ORTHOPAEDIC DIV.
Manufacturer Address1450 BROOKS RD. MEMPHIS TN 38116 US


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2007-04-30

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