Device recall
Z-2236-2016: GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A…
FDA device recall · Class II · GE Inspection Technologies, LP
Key facts
| Recall number (Z-number) | Z-2236-2016 |
|---|---|
| Recall event | 74554 |
| Product | GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis. |
| Product code | RCE |
| Recalling firm | GE Inspection Technologies, LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 7, 2017 |
| FEI number | 2519904 |
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