Recall Z-1851-2019— Tecan US, Inc.
Class II · Terminated
Class II FDA medical device recall by Tecan US, Inc., initiated 2019-04-12, terminated 2022-01-18. FDA's recall record names no specific 510(k) clearance for this event. 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: Gas springs not always replaced within the interval specified..
- Recalling firm
- Tecan US, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-04-12
- Terminated
- 2022-01-18
- Firm location
- Morrisville, NC, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.