Device recall
Z-2233-2025: LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh…
FDA device recall · Class II · Fresenius Kabi USA, LLC
Key facts
| Recall number (Z-number) | Z-2233-2025 |
|---|---|
| Recall event | 97165 |
| Product | LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20. |
| Product code | FRN |
| Recalling firm | Fresenius Kabi USA, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K183311 |
| FEI number | 3014732157 |
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