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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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29 records meeting your search criteria returned- Product Code: OQI Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
CORIN LTD TRINITY 08/10/2023
CORIN LTD TRINITY 07/27/2023
CORIN LTD TRINITY 07/20/2023
BIOMET FRANCE S.A.R.L. GTS STANDARD FMRL STEM SIZE +4 06/15/2023
ZIMMER SWITZERLAND MANUFACTURING GMBH METASUL-FEMORAL HEAD 38 M 12/19/2022
ZIMMER SWITZERLAND MANUFACTURING GMBH ARTEK CUP ME 38/52 12/19/2022
BIOMET UK LTD. CER OPT TYPE 1 TPR SLEVE 0MM 07/08/2021
BIOMET UK LTD. CER BIOLOXD OPTION HD 28MM 07/08/2021
ZIMMER BIOMET, INC. G7 VIT E NEUTRAL LNR 36MM F 03/16/2021
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