Device recall
Z-2470-2008: Maxi Move Patient Lift with Lock & Load System (Combi Hanger); Manufactured by…
FDA device recall · Class II · Arjo, Inc.
Key facts
| Recall number (Z-number) | Z-2470-2008 |
|---|---|
| Recall event | 49391 |
| Product | Maxi Move Patient Lift with Lock & Load System (Combi Hanger); Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Models KMBB4CLU2FUS, KMBB4MLU2FUS, KMBB4MSU2FUS, KMBB4NLX2FUS, KMBB4NSX2FUS, KMBB4OLU2FUS, KMBB4OSU2FUS, KMBB4PLX2FUS, KMBB4PSX2FUS, KMBB4QLU2FUS, and KMBB4RLX2FUS. The lifter is… |
| Product code | FSA |
| Recalling firm | Arjo, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2011 |
| FEI number | 1419652 |
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