Device recall
Z-2312-2012: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended to be…
FDA device recall · Class II · Capintec Inc
Key facts
| Recall number (Z-number) | Z-2312-2012 |
|---|---|
| Recall event | 62982 |
| Product | Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended to be used by trained Nuclear Medicine Technologists to perform thyroid uptake procedures, which consist of the measurement of organ uptake and circulating radioactivity. |
| Product code | IZD |
| Recalling firm | Capintec Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2013 |
| FEI number | 2518443 |
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