# FDA recall Z-1446-2020

> **Covidien Llc** · Class II · device recall initiated 2020-02-10.

## Product

Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084  20884524000081; 10884524001937  20884524001934

## Reason for recall

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

## Distribution

Nationwide domestic distribution. Foreign distribution to Australia, Canada, Austria  Belgium  Canary Islands  Czech Republic  Denmark  Finland  France  Germany  Greece  Hungary  Italy  Jordan  Kazakhstan  Kenya  Lithuania  Luxembourg  North Macedonia  Poland  Portugal  Reunion  Romania  Russian Federation  Serbia  Slovakia  Spain  Sweden  Switzerland  United Kingdom  No U.S. distribution of Kits. Foreign distribution in EMEA  only. (Europe, Middle East and Africa.)

## Key facts

- **Recall number:** Z-1446-2020
- **Recalling firm:** Covidien Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-10
- **Report date:** 2020-03-11
- **Termination date:** 2024-04-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1446-2020

## Citation

> AI Analytics. FDA recall Z-1446-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1446-2020. Source: US FDA. Licensed CC0.

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