Device recall
Z-2734-2014: The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage…
FDA device recall · Class II · Baro-Therapies, Inc
Key facts
| Recall number (Z-number) | Z-2734-2014 |
|---|---|
| Recall event | 69053 |
| Product | The Rejuvenator Chamber manufactured by Baro-Therapies, Inc. Product Usage: Indicated for relief from general aches and pains brought on by changes in the weather. |
| Product code | CBF |
| Recalling firm | Baro-Therapies, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2015 |
| FEI number | 3009829568 |
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