Device recall
Z-1968-2015: Infinite M1000 PRO in vitro diagnostic. Product Usage: The Tecan Infinite M1000…
FDA device recall · Class II · Tecan US, Inc.
Key facts
| Recall number (Z-number) | Z-1968-2015 |
|---|---|
| Recall event | 71352 |
| Product | Infinite M1000 PRO in vitro diagnostic. Product Usage: The Tecan Infinite M1000 PRO is a multifunctional monochromator based microplate reader that provides high performance for the vast majority of todays microplate applications and research. In addition to offering absorbance and fluorescence… |
| Product code | KHO |
| Recalling firm | Tecan US, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2017 |
| 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