Device recall
Z-2096-2025: Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2
FDA device recall · Class I · Baxter Healthcare Corporation
Key facts
| Recall number (Z-number) | Z-2096-2025 |
|---|---|
| Recall event | 97072 |
| Product | Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2 |
| Product code | PHC |
| Recalling firm | Baxter Healthcare Corporation |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K230022 |
| FEI number | 1417572 |
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