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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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216 records meeting your search criteria returned- Product Code: LWJ Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 10/01/2018
ENCORE MEDICAL L.P. CLP HIP 09/14/2018
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 08/07/2018
ZIMMER BIOMET, INC. E-POLY 36MM +3 MAXROM LNR SZ23 08/03/2018
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 07/31/2018
CORIN MEDICAL TRINITY 07/16/2018
STRYKER ORTHOPAEDICS-MAHWAH C-TAPER COCR LFIT HEAD 28MM/+5 05/14/2018
ZIMMER BIOMET, INC. UNKNOWN HEAD 05/10/2018
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 04/20/2018
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 04/04/2018
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