HIGHFDA DEVICE

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.

INSPIREMDHealth & Personal CareMedical DevicesUDI: 07290120281783all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
May 1, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 1, 2026
Hazard Level
HIGH
Brand
INSPIREMD
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
INSPIREMD
Model numbers
UDI: 07290120281783, all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 1, 2026

  2. Reported by FDA DEVICE

    June 17, 2026

  3. RecallRadar source check

    June 23, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact INSPIREMD Inc or your healthcare provider for instructions. Notification method: E-Mail

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Full Description

CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040. Reason: Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.. Classification: Class II. Quantity: 211 units. 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.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
UDI: 07290120281783
all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Affected States
ALL
Report Date
June 17, 2026
Recall Status
ACTIVE

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