Device recall
Z-3162-2024: Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting…
FDA device recall · Class II · Btt Health Gmbh
Key facts
| Recall number (Z-number) | Z-3162-2024 |
|---|---|
| Recall event | 95233 |
| Product | Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment |
| Product code | BXB |
| Recalling firm | Btt Health Gmbh |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3013515165 |
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