ACETABLR CUP HAP 74120144

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-24 for ACETABLR CUP HAP 74120144 manufactured by Smith & Nephew Orthopaedics Ltd.

Event Text Entries

[184677071] It was reported a right hip revision surgery was performed due to persistent pain and discomfort in right hip, felt a warm fluid-like sensation in the hip, heard audible popping and felt a painful grinding sensation in the right hip. In addition, patient has elevated metal ion levels in blood.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005975929-2020-00083
MDR Report Key9872271
Date Received2020-03-24
Date of Report2020-03-24
Date of Event2012-10-30
Date Mfgr Received2020-02-24
Date Added to Maude2020-03-24
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 NameACETABLR CUP HAP
Generic NamePROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/METAL, RESURFACING
Product CodeNXT
Date Received2020-03-24
Catalog Number74120144
Device AvailabilityN
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 2020-03-24

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