Class II

Medical Device Recall: CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040

INSPIREMD Inc · May 1, 2026

Reason for Recall

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Distribution

US Nationwide distribution in the states of AR, AZ, CA, DC, FL, GA, HI, IL, IN, KS, MA, MD, MI, MO, NC, NJ, NV, NY, OH, OR, RI, SD, TN, TX, VA, WA, WI, WV.

States Affected

NATIONWIDE

Quantity Affected

211 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2330-2026

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.