Class II
Medical Device Recall: Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Only
Cordis US Corp · March 4, 2025
Reason for Recall
product mix-up; Vascular stent labeled as one size but contains a different size.
Distribution
US Distribution to states of: AR, AZ, FL, NJ, TN; and OUS Foreign country of: Japan
States Affected
AR, AZ, FL, NJ, TN
Quantity Affected
20 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1510-2025
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.