Class II U.S. Food and Drug Administration

INSPIREMD Inc Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/ recall: Stent delivery system may encounter complications during deployment

Recall published 4 months ago

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

The hazard: Device safety concern

The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

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

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-2328-2026
Published
June 17, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
INSPIREMD Inc
Product type
Medical devices
Units affected
291 units
Distribution
Nationwide
Made in
United States
Lot / code info
UDI: 07290120281745; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
UPC codes
07290120281745

Products covered by this recall

Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940

Check your product

The notice names 12 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 07290120281745

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 03
  • 2025
  • 02
  • 23
  • 2026 — 291 u

Model or item number

On the rating label, the box or the instruction sheet.

  • CND0940 — UDI

Serial number

On the rating plate, often next to the date of manufacture.

  • manufactured between 02
  • 03
  • 2025
  • 02
  • 23

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

INSPIREMD Inc — The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If you are a facility, quarantine affected stock and log the correction.
  3. Report device problems to the FDA through MedWatch.
  4. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.

Who pays for a device recall

The manufacturer funds the remedy. The practical question is usually which link in the chain executes it.

  • If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.
  • Ask for written confirmation that the remedy was applied to your serial number. That is what an insurer or a future clinician will want to see.
  • If you bought it yourself online or from a pharmacy, go to the manufacturer’s recall page rather than the retailer; device claims are handled centrally.
  • Where the remedy is a software update, there is nothing to claim, but do confirm the version changed afterwards.

Company contact: INSPIREMD Inc — 6303 Waterford District Dr Ste 215, Miami, FL, 33126-6004

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was INSPIREMD Inc medical devices recalled?

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

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 07290120281745; lot code 03, 2025, 02; model number CND0940 — UDI. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.

Where was the recalled product sold?

It was distributed nationwide.

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