Reported Mar 11, 2020 · Terminated

Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084…

Covidien LLC

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 Llc · 15 Hampshire St · Mansfield, MA · 02048-1113

Is this the product you have?

  • Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934
Lot codes and dates
  • Lots

    80 of 80 codes

    • 181170378R
    • 181170379R
    • 181170380R
    • 192100010R
    • 192170108R
    • 192170109R
    • 192240106R
    • 192240107R
    • 192240108R
    • 192630089R
    • 192100011R
    • 192660102R
    • 192450230R
    • 192660103R
    • 192800040R
    • 190530412R
    • 190530413R
    • 190600130R
    • 190630011R
    • 190640010R
    • 190880338R
    • 190880339R
    • 190880340R
    • 190880341R
    • 191020334R
    • 191160340R
    • 191160342R
    • 191300316R
    • 191300317R
    • 191370322R
    • 191370323R
    • 191510192R
    • 191440287R
    • 191510193R
    • 191580245R
    • 191580246R
    • 191580247R
    • 191650218R
    • 191650219R
    • 191720261R
    • 191790222R
    • 191790223R
    • 191790224R
    • 191860195R
    • 191860197R
    • 191090309R
    • 191090310R
    • 191440286R
    • 191930105R
    • 191930107R
    • 191930108R
    • 192170106R
    • 192170107R
    • 191720259R
    • 192000197R
    • 192000200R
    • 192070039R
    • 192100007R
    • 192070038R
    • 191160341R
Amount recalled
70361

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 26, 2024 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.