# FDA recall Z-0631-2024

> **Covidien** · Class II · device recall initiated 2023-11-16.

## Product

Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD

## Reason for recall

Due to software issue, New systems may exhibit an error which may prohibit use of new systems resulting in system being inoperable

## Distribution

Worldwide distribution - US: Nationwide and surrounding territories.

## Key facts

- **Recall number:** Z-0631-2024
- **Recalling firm:** Covidien
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-16
- **Report date:** 2024-01-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lafayette, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0631-2024

## Citation

> AI Analytics. FDA recall Z-0631-2024. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-0631-2024. Source: US FDA. Licensed CC0.

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