Device recall
Z-0619-2024: Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111
FDA device recall · Class III · Fresenius Medical Care Holdings, Inc.
Key facts
| Recall number (Z-number) | Z-0619-2024 |
|---|---|
| Recall event | 93579 |
| Product | Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111 |
| Product code | FKX |
| Recalling firm | Fresenius Medical Care Holdings, Inc. |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K222318 |
| FEI number | 3001451489 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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