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
181170378R181170379R181170380R192100010R192170108R192170109R192240106R192240107R192240108R192630089R192100011R192660102R192450230R192660103R192800040R190530412R190530413R190600130R190630011R190640010R190880338R190880339R190880340R190880341R191020334R191160340R191160342R191300316R191300317R191370322R191370323R191510192R191440287R191510193R191580245R191580246R191580247R191650218R191650219R191720261R191790222R191790223R191790224R191860195R191860197R191090309R191090310R191440286R191930105R191930107R191930108R192170106R192170107R191720259R192000197R192000200R192070039R192100007R192070038R191160341R
- Lots
- 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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