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INSPIREMD Inc recalls CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930
Recalled June 17, 2026 · FDA recall Z-2327-2026 · INSPIREMD
Hazard
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. · FDA Class II
Units
147 units
Sold at
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.
Description
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Product
CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930
Manufacturer(s)
INSPIREMD Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →