FDA recall Z-3258-2026

INTERVASCULAR, SAS · Class II · device

Product

Cardioroot Woven Collagen Coated Vascular Graft; Model Numbers: 1. HEWROOT0024, 2. HEWROOT0026, 3. HEWROOT0028, 4. HEWROOT0030, 5. HEWROOT0032, 6. HEWROOT0034;

Reason for recall

Product failed to meet the specified acceptance criteria for Integral Water Permeability (IWP).

Distribution

Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Argentina, Australia, Austria, Belgium, Bulgaria, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Jordan, Kenya, Kosovo, Kuwait, Latvia, Luxembourg, Malaysia, Mauritius, Monaco, Netherlands, New Zealand, Nicaragua, Nigeria, Norway, Oman, Poland, Portugal, Qatar, Romania, Russia, Saudi Arabia, Serbia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Tunisia, Turkey, United Arab Emirates, United Kingdom, Yemen.

Key facts

Status
Ongoing
Initiation date
2026-08-12
Report date
2026-09-30
Voluntary/Mandated
Voluntary: Firm initiated
Location
La Ciotat Cedex, France

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3258-2026