Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy Recalled by Covidien, PLC Due to Potential for the sterile packaging to be compromised
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, PLC directly.
Affected Products
Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such as general, urologic, thoracic, plastic and reconstructive, gynecologic) and minimally invasive arthroscopic procedures where the surgeon desires monopolar radio-frequency electrosurgical energy to cut and/or coagulate tissue. The electrosurgical device is intended for use with conventional monopolar electrosurgical electrodes. Item Code: FT3000F
Quantity: 850 units
Why Was This Recalled?
Potential for the sterile packaging to be compromised
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien, PLC
Covidien, PLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report