CGuard Prime Carotid Stent System: recall status ⚠ Recalls found. CGuard Prime Carotid Stent System is named in 3 official recalls in our current data:
FDA Class II recall Z-2327-2026 — Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.FDA Class II recall Z-2329-2026 — Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.FDA Class II recall Z-2330-2026 — Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. Source checks: October 22, 2026 at 6:00 PM UTC (oldest successful check).
Sources, dates and coverage limits We collect recent notices on a six-hour schedule using a rolling 90-day source request. Older retained records may also appear. This is a recall index, not a catalogue of all products or a complete recall history.
CPSC: stored recall dates April 30, 2026 to October 22, 2026. NHTSA: stored recall dates April 24, 2026 to October 19, 2026. FDA: stored recall dates April 29, 2026 to October 14, 2026. USDA FSIS is not aggregated here. Check USDA meat, poultry and processed egg notices . EPA and U.S. Coast Guard are not aggregated. Source delays and missing identifiers can prevent a match.
Brand INSPIREMD Also listed as CGuard¿ Prime Carotid Stent System Recalls naming this model FDA Class II · Medical device · June 17, 2026
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: CGuard Prime Carotid Stent System recall status
Official ID Z-2327-2026 ·
Official record ↗
FDA Class II · Medical device · June 17, 2026
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: CGuard Prime Carotid Stent System recall status
Official ID Z-2329-2026 ·
Official record ↗
FDA Class II · Medical device · June 17, 2026
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: CGuard¿ Prime Carotid Stent System recall status
Official ID Z-2330-2026 ·
Official record ↗
See all INSPIREMD recalls →
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.