Device recall
Z-1431-2012: Zuma Mobility System Models: Zuma Mobility Assist 412045-01 and Zuma Mobility…
FDA device recall · Class II · KCI USA, Inc.
Key facts
| Recall number (Z-number) | Z-1431-2012 |
|---|---|
| Recall event | 61547 |
| Product | Zuma Mobility System Models: Zuma Mobility Assist 412045-01 and Zuma Mobility Trainer 412046-01. Product Usage: Human Non-AC-Powered Patient Lift |
| Product code | FSA |
| Recalling firm | KCI USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 19, 2012 |
| FEI number | 1625774 |
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