Device recall
Z-1343-2013: Molift Smart 150
FDA device recall · Class II · Moller Vital
Key facts
| Recall number (Z-number) | Z-1343-2013 |
|---|---|
| Recall event | 64512 |
| Product | Molift Smart 150 |
| Product code | FSA |
| Recalling firm | Moller Vital |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2014 |
| FEI number | 3004137175 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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