Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo Cardiovascular Systems Corporation Due to Sterility of medical devices intended for use in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Terumo Cardiovascular Systems Corporation directly.
Affected Products
VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System, Part number: VSP550, Sterile***Rx Only*** Product Usage: The VirtuoSaph Plus Endoscopic Vessel Harvesting System is indicated for use in minimally invasive surgery allowing access for vessel harvesting, and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass.
Quantity: 26 units
Why Was This Recalled?
Sterility of medical devices intended for use in surgical procedures may be compromised.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Terumo Cardiovascular Systems Corporation
Terumo Cardiovascular Systems Corporation has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report