Device recall
Z-2721-2024: LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port…
FDA device recall · Class I · Fresenius Kabi USA, LLC
Key facts
| Recall number (Z-number) | Z-2721-2024 |
|---|---|
| Recall event | 95113 |
| Product | LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25), Product Code: SET-0013-25. for intravenous infusion. |
| Product code | FPA |
| Recalling firm | Fresenius Kabi USA, LLC |
| Recall class | Class I |
| 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
- 1,000+ 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