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Terminated

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.

FDA Recall Z-1851-2019 · Posted None

Recalling FirmTecan US, Inc.
Recall StatusTerminated
Product CodeJQW
Date Initiated2019-04-12
Date Terminated2022-01-18
Product Quantity40

Reason for Recall

Gas springs not always replaced within the interval specified.

Firm Action

In April 2019, Tecan US sent Field Corrective Action Freedom EVO 200 letters to their US and Canadian consignees advising them of the issue; requesting that they complete and return an acknowledgement receipt; to pass the letter to any organization where the devices may be transferred and to arrange for a Tucan US representative to replace the gas springs

Root Cause

Under Investigation by firm

Distribution Pattern

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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