DELTA 76539153

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 2012-06-15 for DELTA 76539153 manufactured by Smith&nephew - Germany.

Event Text Entries

[2727716] It was reported that a revision surgery was performed due to dislocation.
Patient Sequence No: 1, Text Type: D, B5


[9927324] .
Patient Sequence No: 1, Text Type: N, H10


[21147475] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1020279-2012-00345
MDR Report Key2618406
Report Source07
Date Received2012-06-15
Date of Report2012-05-28
Date of Event2012-05-28
Date Mfgr Received2012-07-08
Device Manufacturer Date2007-11-01
Date Added to Maude2012-06-18
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 ContactMR PHILLIP EMMERT
Manufacturer Street1450 E. BROOKS RD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013995296
Manufacturer G1SMITH&NEPHEW - GERMANY
Manufacturer StreetALEMANNENSTRASSE 14
Manufacturer CityTUTTLINGEN 78532
Manufacturer CountryGM
Manufacturer Postal Code78532
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDELTA
Generic NameFEMORAL HEAD COMPONENT
Product CodeLPF
Date Received2012-06-15
Catalog Number76539153
Lot Number07LT14450A
Device Expiration Date2017-11-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH&NEPHEW - GERMANY
Manufacturer AddressALEMANNENSTRASSE 14 TUTTLINGEN 78532 GM 78532


Patients

Patient NumberTreatmentOutcomeDate
1713317541. Hospitalization; 2. Required No Informationntervention 2012-06-15

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