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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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412 records meeting your search criteria returned- Product Code: JDG Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. UNKN FEM HEAD MEMPHIS OX 02/08/2022
SMITH & NEPHEW, INC. UNKN ORTHOPAEDIC RECONSTRUCTION DEV 02/01/2022
SMITH & NEPHEW, INC. UNKN ORTHOPAEDIC RECONSTRUCTION DEV 02/01/2022
SMITH & NEPHEW, INC. R3 36MM ID INTL DLT CER LNR 52MM 02/01/2022
SMITH & NEPHEW ORTHOPAEDICS AG EP-FIT/MPF CERAMIC INSERT DELTA 52/32 01/20/2022
SMITH & NEPHEW, INC. TNDM BP SHL/XLPE LNR 45OD 26ID 01/18/2022
SMITH & NEPHEW, INC. UNKN SMITH+NEPHEW DEV 01/10/2022
SMITH & NEPHEW, INC. UNKN ORTHOPAEDIC RECONSTRUCTION DEV 01/10/2022
SMITH & NEPHEW, INC. REF XLPE 32 20 DEG 50-52 E 11/16/2021
SMITH & NEPHEW, INC. UNKN MEMPHIS RECON KNEE INSTR 11/16/2021
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