Device recall
Z-1825-2011: Phoenix x/ray analyser series. Phoenix x|ray analyser series cabinet x-ray…
FDA device recall · Class II · GE Inspection Technologies, LP
Key facts
| Recall number (Z-number) | Z-1825-2011 |
|---|---|
| Recall event | 52193 |
| Product | Phoenix x/ray analyser series. Phoenix x|ray analyser series cabinet x-ray systems are used in non-destructive testing, failure analysis, process control, and metrology. |
| Product code | RCE |
| Recalling firm | GE Inspection Technologies, LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 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