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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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282 records meeting your search criteria returned- Product Code: MEH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
STRYKER ORTHOPAEDICS-MAHWAH RESTORATION ADM X3 INS 28/48 03/08/2022
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 5 02/22/2022
CORIN MEDICAL TRINITY 02/15/2022
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 6 02/14/2022
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 4 02/03/2022
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN REJUVENATE MODULAR NECK 01/31/2022
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN REJUVENATE MODULAR STEM 01/31/2022
CORIN MEDICAL TRINITY 01/28/2022
DEPUY IRELAND - 9616671 UNK HIP FEMORAL STEM ACTIS 01/27/2022
DEPUY ORTHOPAEDICS INC US ACTIS COLLARED HIGH SIZE 9 01/27/2022
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