# FDA recall Z-1851-2019

> **Tecan US, Inc.** · Class II · device recall initiated 2019-04-12.

## Product

Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and general purpose liquid handling and robotic processes.

## Reason for recall

Gas springs not always replaced within the interval specified.

## Distribution

Worldwide distribution. US Nationwide distribution in the states CA, CO, CT, KS, NC, NJ, OR, RI, TN, TX, and VA. Country of Canada.

## Key facts

- **Recall number:** Z-1851-2019
- **Recalling firm:** Tecan US, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-12
- **Report date:** 2019-07-03
- **Termination date:** 2022-01-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1851-2019

## Citation

> AI Analytics. FDA recall Z-1851-2019. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1851-2019. Source: US FDA. Licensed CC0.

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