🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: May 1, 2026 INSPIREMD Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI: 07290120281738; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
INSPIREMD Inc
Reason for Recall:
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

UDI: 07290120281738; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2327-2026

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