Device recall
Z-1335-2012: U-SPECT-II/CT and VECTor/CT cabinet x-ray products. Laboratory research using…
FDA device recall · Class II · Milabs Bv
Key facts
| Recall number (Z-number) | Z-1335-2012 |
|---|---|
| Recall event | 61499 |
| Product | U-SPECT-II/CT and VECTor/CT cabinet x-ray products. Laboratory research using small animals. |
| Product code | RFK |
| Recalling firm | Milabs Bv |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 29, 2012 |
| FEI number | 3008406612 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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