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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 7 12/22/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 3 12/21/2020
STRYKER ORTHOPAEDICS-MAHWAH OMNIFLEX M-HA HIP STEM 12/18/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 5 12/09/2020
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD44MM 12/09/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 7 12/08/2020
ORTHO DEVELOPMENT ALPINE 12/07/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 4 12/05/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 5 12/04/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 9 11/30/2020
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