medical MODERATE Updated 2026-06-17

INSPIREMD Inc recalls Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx4

See all recalls from INSPIREMD Inc →

Recalled Product

Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: 07290120281707; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Brand Name: CGuard¿ Prime →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

INSPIREMD Inc recalls CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/

2026-06-17 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

BERLIN HEART GMBH recalls EXCOR Pediatric Ventricular Assist Device (VAD) System Blood

2026-06-17 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.

Abbott Medical recalls Merlin" Patient Care System (PCS) software Merlin" PCS 3650

2026-06-17 · Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.

GE Medical Systems, LLC recalls Allia IGS 7 Pulse angiographic X-ray system

2026-06-17 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.