Device recall
Z-1753-2013: Hydra Vision DR 60/80 System, Models 700539 and 700540, Liebel-Flarshiem…
FDA device recall · Class II · Leibel-Flarsheim Company LLC
Key facts
| Recall number (Z-number) | Z-1753-2013 |
|---|---|
| Recall event | 65176 |
| Product | Hydra Vision DR 60/80 System, Models 700539 and 700540, Liebel-Flarshiem Company. The System is used in radiologic imaging procedures. |
| Product code | OWB |
| Recalling firm | Leibel-Flarsheim Company LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2013 |
| 510(k) numbers | K943581 |
| FEI number | 1518293 |
At a glance
- 1–9 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