Device recall
Z-0201-2009: Vibe Technologies, VIBE machine, Vibrational Integrated Biophotonic Energizer.
FDA device recall · Class I · VIBE Technologies
Key facts
| Recall number (Z-number) | Z-0201-2009 |
|---|---|
| Recall event | 49590 |
| Product | Vibe Technologies, VIBE machine, Vibrational Integrated Biophotonic Energizer. |
| Recalling firm | VIBE Technologies |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 21, 2012 |
| FEI number | 3004494240 |
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