Recall
FDAHealthMay 1, 2026

INSPIREMD Inc — Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 1, 2026

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.

What's affected?

Product
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Lot code
/serial

Additional details

UDI: 07290120281691; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 190 units.

View original FDA notice →

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