Device recall
Z-1141-2012: Arasys Product Usage: Muscle stimulation
FDA device recall · Class II · Ion Genius, Inc.
Key facts
| Recall number (Z-number) | Z-1141-2012 |
|---|---|
| Recall event | 61073 |
| Product | Arasys Product Usage: Muscle stimulation |
| Product code | IPF |
| Recalling firm | Ion Genius, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 21, 2015 |
| FEI number | 3003588228 |
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