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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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74 records meeting your search criteria returned- Product Code: JDI Patient Problem: Sepsis Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN FEMORAL STEM 12/06/2018
ZIMMER BIOMET, INC. UNKNOWN BONE SCREW 12/06/2018
ZIMMER BIOMET, INC. UNKNOWN LINER 12/06/2018
ZIMMER BIOMET, INC. UNKNOWN LINER 12/06/2018
ZIMMER BIOMET, INC. UNKNOWN FEMORAL HEAD 12/06/2018
ZIMMER BIOMET, INC. UNKNOWN SCREW 12/06/2018
ZIMMER BIOMET, INC. UNKNOWN FEMORAL HEAD 12/06/2018
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL AUGMENT 12/05/2018
ZIMMER BIOMET, INC. M2A-MAGNUM MOD HD SZ 44MM 11/01/2018
DEPUY ORTHOPAEDICS, INC. 1818910 ARTICULEZE M HEAD 36MM +1.5 08/28/2018
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