Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1851-2019 — 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.

U.S. FDA — Device Enforcement · United States · 2019-04-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1851-2019
Date of alert: 2019-04-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Tecan US, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10641200

Reported risk: Gas springs not always replaced within the interval specified.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1851-2019 — 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.

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