R3 42MM ID INTL COCR LINER 54MM 71335854

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-17 for R3 42MM ID INTL COCR LINER 54MM 71335854 manufactured by Smith & Nephew Orthopaedics Ltd.

Event Text Entries

[179710864] It was reported that a revision surgery was performed due to consistent pain. Liner, head and sleeve exchanged.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005975929-2020-00057
MDR Report Key9716758
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-17
Date of Report2020-02-17
Date of Event2020-02-10
Date Mfgr Received2020-02-10
Device Manufacturer Date2008-09-30
Date Added to Maude2020-02-17
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 Location3
Manufacturer ContactDR. SARAH FREESTONE
Manufacturer G1SMITH & NEPHEW ORTHOPAEDICS LTD
Manufacturer StreetAURORA HOUSE SPA PARK
Manufacturer CityLEAMINGTON SPA CV313HL
Manufacturer CountryUK
Manufacturer Postal CodeCV31 3HL
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameR3 42MM ID INTL COCR LINER 54MM
Generic NamePROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/METAL, RESURFACING
Product CodeNXT
Date Received2020-02-17
Catalog Number71335854
Lot Number08JW18739
Device Expiration Date2018-09-28
OperatorLAY USER/PATIENT
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW ORTHOPAEDICS LTD
Manufacturer AddressAURORA HOUSE SPA PARK LEAMINGTON SPA CV313HL UK CV31 3HL


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2020-02-17

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