ALUM CER LNR 32ID 56-66 71338456

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2011-02-10 for ALUM CER LNR 32ID 56-66 71338456 manufactured by Smith & Nephew Orthopaedics, Inc..

Event Text Entries

[1729140] It was reported that surgery time was extended due to breakage of the device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1020279-2011-00034
MDR Report Key1983538
Report Source07
Date Received2011-02-10
Date of Report2011-02-10
Date of Event2010-12-21
Date Mfgr Received2011-01-11
Device Manufacturer Date2006-02-01
Date Added to Maude2011-02-10
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 FDA0
Event Location0
Manufacturer ContactCARLA SAMUELS
Manufacturer Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013995076
Manufacturer G1SMITH & NEPHEW ORTHOPAEDICS, 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 NameALUM CER LNR 32ID 56-66
Generic NameCERAMIC LINER
Product CodeLPF
Date Received2011-02-10
Model Number71338456
Catalog Number71338456
Lot Number06BM06912A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
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 2011-02-10

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