Device recall
Z-2291-2016: Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC…
FDA device recall · Class II · Moller Vital
Key facts
| Recall number (Z-number) | Z-2291-2016 |
|---|---|
| Recall event | 74529 |
| Product | Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC Propulsion, Molift Air 300, Molift Air 300 Propulsion, Molift Air 300 IRC, Molift Air 300 IRC Propulsion Molift Air is a ceiling hoist used to lift and transfer immobilized patients in various situations. The coupling that… |
| Product code | FSA |
| Recalling firm | Moller Vital |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2017 |
| 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