Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Recalled by Covidien LP Due to Seals may disengage from the cannula which may...
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 Covidien LP directly.
Affected Products
Versaport Bladeless Optical Trocar With (2) Fixation Cannulae - 5mm Product Code: ONB5STF2C The Versaport" Bladeless Optical 5mm trocars are intended for use in a variety of gynecologic, general, thoracic and urologic endoscopic procedures to create and maintain a port of entry.
Quantity: 5364 units
Why Was This Recalled?
Seals may disengage from the cannula which may result in a component inadvertently disengaging into the patients cavity
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien LP
Covidien LP has 57 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report