R3 0 DEG +4 XLPE ACET LNR 40MM X 58 OD 71338696

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-12-27 for R3 0 DEG +4 XLPE ACET LNR 40MM X 58 OD 71338696 manufactured by Smith & Nephew, Inc..

Event Text Entries

[173176356] It was reported that a left hip revision surgery was performed due to instability.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1020279-2019-04611
MDR Report Key9528204
Date Received2019-12-27
Date of Report2020-03-11
Date of Event2016-08-30
Date Mfgr Received2020-03-06
Device Manufacturer Date2010-04-07
Date Added to Maude2019-12-27
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 Street1450 BROOKS ROAD
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
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 0 DEG +4 XLPE ACET LNR 40MM X 58 OD
Generic NamePROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, POROUS
Product CodeMBL
Date Received2019-12-27
Model Number71338696
Catalog Number71338696
Lot Number10DM03175
Device Expiration Date2020-04-04
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address1450 BROOKS ROAD MEMPHIS TN 38116 US 38116


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-12-27

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