Reported Mar 27, 2019 · Terminated

Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate…

Covidien, PLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Covidien, PLC · 5920 Longbow Dr · Boulder, CO · 80301-3202

Is this the product you have?

  • Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue
  • Product UsageSingle-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 CodeFT3000F
Lot codes and dates
  • Lot Number80390309X UDI-Device Identifier (GTIN/UPN) 10884524000084/ 20884524000081
Amount recalled
850 units

Where it was sold

  • Nationwide

Why it was recalled

Potential for the sterile packaging to be compromised

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 17, 2020 · Data as of Sep 19, 6:54 PM UTC

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