# FDA device recall: CGuard Prime Carotid Stent System,  135cm, 9mx30mm  Model/Catalog Number: CND0930

> recall · VERIFIED · 2026-05-01

Firm: INSPIREMD Inc · Class II · Stent delivery system may encounter complications during deployment which may result in high resistance  or inability to deploy the stent.

- Company: INSPIREMD Inc
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.