Recalls · Brand

INTERVASCULAR, SAS recalls

Every recall we track for INTERVASCULAR, SAS — 1 in all, all from 2026 — plus the complaints and injury reports the public filed about them.

1recalls

What to do if you have a recalled INTERVASCULAR, SAS product

Match the model, catalog or lot number on your device to the recall.
Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
Report problems to FDA MedWatch.

See this week’s new recalls.

All INTERVASCULAR, SAS recalls

1 shown

ℹ️ UnratedMedical device
INTERVASCULAR, SAS recalls Cardioroot Woven Collagen Coated Vascular Graft; Model Numbers: 1. HEWROOT0024, 2. HEWROOT0026, 3. HEWROOT0028, 4.
Intervascular recalls Cardioroot Woven Collagen Coated Vascular Grafts with model numbers HEWROOT0024-0034 due to failure in water permeability testing. Affected products may not meet quality standards.
IntervascularAug 12, 2026

INTERVASCULAR, SAS recall questions

How many recalls has INTERVASCULAR, SAS had?

1 recall from INTERVASCULAR, SAS are on record with U.S. safety agencies, from 2026.

What is the most recent INTERVASCULAR, SAS recall?

INTERVASCULAR, SAS recalls Cardioroot Woven Collagen Coated Vascular Graft; Model Numbers: 1. HEWROOT0024, 2. HEWROOT0026, 3. HEWROOT0028, 4., dated Aug 12, 2026. Every INTERVASCULAR, SAS recall is listed on this page, newest first.

What should I do if I have a recalled INTERVASCULAR, SAS product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new INTERVASCULAR, SAS recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.