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U.S. Department of Health and Human Services

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

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ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 4 02/12/2021
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD44MM 01/22/2021
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 46MM 01/20/2021
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD44MM 01/13/2021
DEPUY FRANCE SAS - 3003895575 CORAIL2 LAT COXA VARA SIZE 18 01/12/2021
DEPUY IRELAND - 9616671 UNK HIP FEMORAL STEM ACTIS 01/11/2021
STRYKER ORTHOPAEDICS-MAHWAH UNITRAX MODULAR ENDO HEAD 46MM 01/08/2021
SMITH & NEPHEW ORTHOPAEDICS AG UNKN. FRACTURE HEAD 01/07/2021
SMITH & NEPHEW ORTHOPAEDICS LTD UNKN BIRMINGHAM HIP MODULAR HEAD (BHMH) 12/31/2020
DEPUY ORTHOPAEDICS INC US ACTIS COLLARED HIGH SIZE 9 12/29/2020
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