Class II
Medical Device Recall: Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
Encore Medical, LP · January 15, 2026
Reason for Recall
Knee and Humeral socket implants contain incorrect labeling.
Distribution
US Nationwide distribution in the states of VA, TN, IL, IN, MI, CO, WY, MT, RI, MA, NJ, PA, MO, OK, LA, FL, CA.
States Affected
NATIONWIDE
Quantity Affected
14 implants
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1459-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.