Device recall
Z-1310-2014: TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation…
FDA device recall · Class III · Technidata S.A.
Key facts
| Recall number (Z-number) | Z-1310-2014 |
|---|---|
| Recall event | 67628 |
| Product | TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a connected instrument and sends them to a Laboratory Information System (LIS). |
| Product code | JQP |
| Recalling firm | Technidata S.A. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 31, 2014 |
| FEI number | 3003995437 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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