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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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13 records meeting your search criteria returned- Product Code: PHX Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
FX SOLUTIONS HUMELOCK REVERSED 01/05/2022
ENCORE MEDICAL L.P. RSP 06/24/2021
TORNIER INC AEQUALIS PERFORM REVERSED 12/02/2020
ARTHREX, INC. UNIVERS REVERS APEX STEM, SIZE 10 10/30/2020
ARTHREX, INC. UNIVERS REVS CUP,36/NEUTRAL CTD 10/28/2020
ARTHREX, INC. UNI GLENOID-PERIPHERAL LOCK SCRW 10/28/2020
ARTHREX, INC. UNI GLENOID-PERIPHERAL LOCK SCRW 10/28/2020
ARTHREX, INC. UNIVERSAL GLENOID - BASEPLATE SMALL 10/28/2020
ENCORE MEDICAL L.P RSP 10/22/2020
FX SOLUTIONS HUMERIS 08/26/2020
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