Device recall
Z-2464-2008: Nebion H LX-8 magnetic resonance device and stand. Most devices, as they are…
FDA device recall · Class I · Nebion, LLC
Key facts
| Recall number (Z-number) | Z-2464-2008 |
|---|---|
| Recall event | 48967 |
| Product | Nebion H LX-8 magnetic resonance device and stand. Most devices, as they are prototypes, have no labeling, If they are labeled, it is simply as Nebion H LX-8 |
| Recalling firm | Nebion, LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 10, 2011 |
| FEI number | 3006983653 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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