Device recall
Z-2315-2008: Universal SlingBar 350 Product Number: 3156074 Used with the: Viking XS, Viking…
FDA device recall · Class II · Liko AB
Key facts
| Recall number (Z-number) | Z-2315-2008 |
|---|---|
| Recall event | 48747 |
| Product | Universal SlingBar 350 Product Number: 3156074 Used with the: Viking XS, Viking S, Viking M, Viking L Patient Lifts |
| Product code | FSA |
| Recalling firm | Liko AB |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2015 |
| FEI number | 6884 |
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