Device recall
Z-1851-2019: Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks…
FDA device recall · Class II · Tecan US, Inc.
Key facts
| Recall number (Z-number) | Z-1851-2019 |
|---|---|
| Recall event | 82822 |
| 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. |
| Product code | JQW |
| Recalling firm | Tecan US, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 18, 2022 |
| FEI number | 1037985 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database