Z-2326-2026 Class II Ongoing

Recalled by INSPIREMD Inc — Miami, FL

Recall Details

Product Type
Devices
Report Date
June 17, 2026
Initiation Date
May 1, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
424 units

Product Description

Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840

Reason for Recall

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

Distribution Pattern

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.

Code Information

UDI: 07290120281707; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026