Medical Device Recall: Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-5255
CORIN MEDICAL, LTD. · May 23, 2025
Reason for Recall
Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches.
Product Description
Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243
Distribution
US Nationwide distribution in the states of CA, CO, FL, IL, OK, TX, UT.
States Affected
NATIONWIDE
Quantity Affected
341 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2069-2025
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.