Device recall
Z-1743-2013: TDHistology/Cytology Classification name: Calculator/data processing module for…
FDA device recall · Class III · Technidata S.A.
Key facts
| Recall number (Z-number) | Z-1743-2013 |
|---|---|
| Recall event | 65652 |
| Product | TDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862.2100). Intended use: Laboratory Information System (L.I.S) |
| Product code | JQP |
| Recalling firm | Technidata S.A. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 29, 2013 |
| 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