Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Covidien Force TriVerse Electrosurgical Devices Recalled by Covidien Llc Due to Sterile packaging may potentially be compromised, and use...
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 Llc directly.
Affected Products
Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934
Quantity: 70361
Why Was This Recalled?
Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien Llc
Covidien Llc has 59 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report