--- title: "INSPIREMD Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search INSPIREMD Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/inspiremd-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # INSPIREMD Inc recall records **6** reported ongoing 6 records in this archive. Latest source date May 1, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 1, 2026 FDA device enforcement ### [Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830](https://isitonrecall.com/recall/fda-device-z-2325-2026-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. Class II Reported ongoing 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. [Official source for Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2325-2026%22) May 1, 2026 FDA device enforcement ### [Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840](https://isitonrecall.com/recall/fda-device-z-2326-2026-brand-name-cguard-prime-carotid-stent-system-135cm-8mmx40mm-model-catalog-number-cnd0840/) Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Class II Reported ongoing 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. [Official source for Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2326-2026%22) May 1, 2026 FDA device enforcement ### [CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930](https://isitonrecall.com/recall/fda-device-z-2327-2026-cguard-prime-carotid-stent-system-135cm-9mx30mm-model-catalog-number-cnd0930/) Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Class II Reported ongoing 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. [Official source for CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2327-2026%22) May 1, 2026 FDA device enforcement ### [Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940](https://isitonrecall.com/recall/fda-device-z-2328-2026-brand-name-cguard-prime-carotid-stent-system-135cm-9mx40mm-model-catalog-number-cnd0940/) Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Class II Reported ongoing 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. [Official source for Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2328-2026%22) May 1, 2026 FDA device enforcement ### [CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030](https://isitonrecall.com/recall/fda-device-z-2329-2026-cguard-prime-carotid-stent-system-135cm-10mmx30mm-model-catalog-number-cnd1030/) Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Class II Reported ongoing 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. [Official source for CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2329-2026%22) May 1, 2026 FDA device enforcement ### [CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040](https://isitonrecall.com/recall/fda-device-z-2330-2026-cguard-prime-carotid-stent-system-135cm-10mmx40mm-model-catalog-number-cnd1040/) Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Class II Reported ongoing 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. [Official source for CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2330-2026%22) ## Reasons in these listed records - Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. These examples come from this result page and are not a ranking of every recall reason. ## Checking INSPIREMD Inc ### Is there a recall on inspiremd inc right now? This archive contains 6 records, including 6 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search INSPIREMD Inc](https://isitonrecall.com/check/?q=INSPIREMD%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)