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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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301 records meeting your search criteria returned- Product Code: MRA Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZIMMER GMBH MS-30®, LATERAL STEM, CEMENTED, 10, TAP 04/25/2024
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 04/19/2024
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 04/02/2024
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 03/26/2024
ZIMMER BIOMET, INC. BONE SCR 6.5X30 SELF-TAP 03/26/2024
SMITH & NEPHEW, INC. UNKNOWN FEMORAL STEM 03/25/2024
STRYKER ORTHOPAEDICS-MAHWAH TRIDENT ALUMINA INSERT 03/12/2024
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,20X15X165 03/07/2024
SMITH & NEPHEW, INC. R3 3 HOLE ACET SHELL 54MM 02/27/2024
SMITH & NEPHEW, INC. ANTHOLOGY HO POROUS SZ 6 02/12/2024
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