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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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10 records meeting your search criteria returned- Product Code: KWB Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNK COTILE SCREW 09/12/2022
ZIMMER BIOMET, INC. UNK COTILE SCREW 09/12/2022
ZIMMER SWITZERLAND MANUFACTURING GMBH SULOX, HEAD, L, 32/+3.5, TAPER 12/14 10/21/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR METAL HEMI 04/14/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR METAL HEMI 01/06/2021
WARSAW ORTHOPEDICS TSRH 09/07/2020
WARSAW ORTHOPEDICS TSRH 07/02/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR POLY/METAL HEMI 09/16/2019
MEDTRONIC SOFAMOR DANEK USA, INC CD HORIZON SPINAL SYSTEM 06/27/2017
MEDTRONIC SOFAMOR DANEK USA, INC CD HORIZON SPINAL SYSTEM 06/27/2017
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