Recall
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.
Tecan US, Inc. · 12 April 2019
- Status
- Recall terminated
- Why, in the FDA's words
- “Gas springs not always replaced within the interval specified.”
- Recall began
- 12 April 2019
- Company
- Tecan US, Inc.
- Device type
- Product code (JQW)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.