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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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3 records meeting your search criteria returned- Product Code: JDZ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDTRONIC SOFAMOR DANEK USA, INC KYPHON® MIXER 04/25/2022
BIOMET FRANCE S.A.R.L. OPTIPAC 80 REFOBACIN BONE CEMENT R-3 09/23/2020
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_LIM_PRODUCT 12/22/2014
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