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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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85 records meeting your search criteria returned- Product Code: HTQ 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 UNK BROACH 02/02/2024
DEPUY IRELAND - 9616671 UNK BROACH 12/19/2023
DEPUY ORTHOPAEDICS INC US DLT TS CER HD 12/14 32MM +1 11/20/2023
DEPUY ORTHOPAEDICS INC US VMP ENDURANCE 80G 11/07/2023
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 1 10/02/2023
DEPUY ORTHOPAEDICS INC US DLT TS CER HD 12/14 32MM +1 04/21/2023
DEPUY ORTHOPAEDICS INC US DLT TS CER HD 12/14 32MM +1 03/31/2023
DEPUY ORTHOPAEDICS INC US DLT TS CER HD 12/14 32MM +1 03/14/2023
DEPUY ORTHOPAEDICS INC US UNK BROACH 11/08/2022
DEPUY ORTHOPAEDICS INC US UNK BROACH 11/08/2022
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