Device recall
Z-0582-2009: QuantumPulse machine. Vibe Technologies, Greeley, CO. The device is used to…
FDA device recall · Class II · VIBE Technologies
Key facts
| Recall number (Z-number) | Z-0582-2009 |
|---|---|
| Recall event | 49609 |
| Product | QuantumPulse machine. Vibe Technologies, Greeley, CO. The device is used to create light wave frequencies to effect cellular activity. |
| Recalling firm | VIBE Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 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