Device recall
Z-0606-2009: Liko AB Uno Lifts, Powered (non-AC) Patient Lift: Old Uno 102: S/N 20001 through…
FDA device recall · Class II · Liko North America Inc
Key facts
| Recall number (Z-number) | Z-0606-2009 |
|---|---|
| Recall event | 50155 |
| Product | Liko AB Uno Lifts, Powered (non-AC) Patient Lift: Old Uno 102: S/N 20001 through 21300 New Uno 102 EM/EE/ES: S/N 30001 through 48100 Production Dates: Manufactured prior to June 26, 2008 Uno 100 and 102 are battery powered mobile lifts, designed to be used in most of the common lifting situations… |
| Product code | FSA |
| Recalling firm | Liko North America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2016 |
| FEI number | 3001451524 |
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