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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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72 records meeting your search criteria returned- Product Code: JDI Product Problem: Device Contamination with Chemical or Other Material Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZIMMER, INC. TRILOGY ACETABULAR SYSTEM POLYETHYLENE L 08/04/2017
ZIMMER, INC. ZIMMER CONTINUUM ACETABULAR SYSTEM, ZIMM 03/24/2017
STRYKER ORTHOPAEDICS-MAHWAH CENTRAX DURATION 26MM X 50MM 02/07/2017
STRYKER ORTHOPAEDICS-MAHWAH CENTRAX DURATION 26MM X 42MM 01/03/2017
STRYKER ORTHOPAEDICS-MAHWAH CENTRAX DURATION 26MM X 43MM 09/09/2016
STRYKER ORTHOPAEDICS-MAHWAH V40 COCR LFIT HEAD 36MM/-5 05/13/2016
ZIMMER, TURPEAUX INDUSTRIAL PARK CPT HIP SYSTEM FEMORAL STEM 05/12/2016
ZIMMER, TURPEAUX INDUSTRIAL PARK ZIMMER CPT FEMORAL STEM 04/13/2016
ZIMMER ZIMMER CPT FEMORAL STEM 04/13/2016
ZIMMER, TURPEAUX INDUSTRIAL PARK CPT FEMORAL STEM 04/12/2016
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