Device recall
Z-0673-06: Tenderlett Adult Lancet, sterile, single use. Red trigger color with incision…
FDA device recall · Class II · International Technidyne Corp
Key facts
| Recall number (Z-number) | Z-0673-06 |
|---|---|
| Recall event | 34461 |
| Product | Tenderlett Adult Lancet, sterile, single use. Red trigger color with incision depth/length of 1.75mm/0.94mm. Manual surgical instrument for general use. |
| Product code | FMK |
| Recalling firm | International Technidyne Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 30, 2006 |
| 510(k) numbers | K923302 |
| FEI number | 2250033 |
At a glance
- 1–9 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