Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe Recalled by Vortex Surgical Inc. Due to Reason for the voluntary recall is some products...
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 Vortex Surgical Inc. directly.
Affected Products
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Quantity: 221 units
Why Was This Recalled?
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Where Was This Sold?
US and Japan
About Vortex Surgical Inc.
Vortex Surgical Inc. has 15 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report