Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to These catheters may have the following deficiencies: 1)...
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 OriGen Biomedical, Inc. directly.
Affected Products
Reinforced Dual Lumen Cannula, 23Fr., REF: VV23F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.
Quantity: 169
Why Was This Recalled?
These catheters may have the following deficiencies: 1) barium sulfate omission, and 2) actual catheter tip length is one centimeter shorter than printed on the tip
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About OriGen Biomedical, Inc.
OriGen Biomedical, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report