Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lots 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 191650217R 191860198R 191930106R 192000198R 192000199R 192520130R 192660097R 192660099R 192660100R 192070041R 192520129R 192380040R 192450224R 192450225R 192450227R 192520131R 192380041R 192600113R 192730131R 192870153R
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Covidien Llc
- Reason for Recall:
- Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934
Product Codes/Lot Numbers:
Lots 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 191650217R 191860198R 191930106R 192000198R 192000199R 192520130R 192660097R 192660099R 192660100R 192070041R 192520129R 192380040R 192450224R 192450225R 192450227R 192520131R 192380041R 192600113R 192730131R 192870153R
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1446-2020
Related Recalls
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A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
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