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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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12 records meeting your search criteria returned- Product Code: LWJ Product Problem: Malposition of Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS AG BICON-PLUS SHELL 09/14/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR MODULAR FEMORAL NECK 01/05/2021
ZIMMER BIOMET, INC. FEMORAL STEM - REVISION TAPER 03/13/2019
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN ACCOLADE I STEM 09/19/2018
DEPUY FRANCE SAS - 3003895575 CORAIL REVISION STEM STD 13 04/26/2018
ZIMMER BIOMET, INC. KINECTIV MODULAR NECK A 10/23/2017
JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.3 SUMMIT BASIC PRESS FIT SZ 4 05/24/2017
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 03/08/2016
STELKAST, INC. PROVIDENT HIP SYSTEM 07/30/2015
DEPUY ORTHOPAEDICS, INC.1818910 UNKNOWN DEPUY SROM CUP 03/30/2015
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