Device recall
Z-1892-2024: Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid…
FDA device recall · Class II · Mirion Technologies (Capintec), Inc.
Key facts
| Recall number (Z-number) | Z-1892-2024 |
|---|---|
| Recall event | 94570 |
| Product | Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests. |
| Product code | IZD |
| Recalling firm | Mirion Technologies (Capintec), Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 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