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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
EXACTECH, INC. ALTEON HPS STD SZ 12 06/30/2022
ZIMMER BIOMET, INC. TPRLC 133 T1 PPS HO 11X142MM 2MM T1 06/29/2022
ZIMMER BIOMET, INC. TPRLC XR FP TYPE1 PPS 7X134MM 06/14/2022
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 50MM 06/03/2022
ZIMMER BIOMET, INC. TPRLC 133 T1 PPS HO 17X154MM 4MM T1 05/31/2022
SMITH & NEPHEW ORTHOPAEDICS LTD HEMI HEAD 40MM 05/21/2022
STRYKER ORTHOPAEDICS-MAHWAH UNITRAX MODULAR ENDO HEAD 47MM 05/11/2022
SMITH & NEPHEW ORTHOPAEDICS LTD UNKNOWN BIRMINGHAM HIP MODULAR HEAD (BHM 05/06/2022
ZIMMER BIOMET, INC. TPRLC 133 FP TYPE1 PPS SO 8.0 05/03/2022
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN OMNIFIT HFX 05/03/2022
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