Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The potential for trocar seal disengagement when using...
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
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BTNL
Quantity: 44,777 units
Why Was This Recalled?
The potential for trocar seal disengagement when using mesh products incorrectly with the device.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien, LP
Covidien, LP has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report