Device recall
Z-2625-2014: Life Force Chamber Product Usage:The product is intended for restful…
FDA device recall · Class II · Life Force of Tampa, LLC
Key facts
| Recall number (Z-number) | Z-2625-2014 |
|---|---|
| Recall event | 69043 |
| Product | Life Force Chamber Product Usage:The product is intended for restful contemplation and spirituality. |
| Product code | LGM |
| Recalling firm | Life Force of Tampa, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 30, 2015 |
| FEI number | 3010406411 |
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