R3

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 2012-09-25 for R3 manufactured by Smith&nephew, Inc..

Event Text Entries

[2907786] It was reported that a revision surgery was performed on the implant for recurrent dislocation. The revision surgeon relates 100% of dislocation on acetabular cup placement. The explant showed good bone ingrowth. The revision surgeon does not fault the device. The implant was approximately 1 year old.
Patient Sequence No: 1, Text Type: D, B5


[10152931] .
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1020279-2012-00536
MDR Report Key2758504
Report Source07
Date Received2012-09-25
Date of Report2012-09-11
Date of Event2012-09-11
Date Mfgr Received2012-09-11
Date Added to Maude2012-09-25
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, 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 NameR3
Generic NameACETABULAR SHELL
Product CodeLPF
Date Received2012-09-25
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
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 2012-09-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.