Device recall
Z-2165-2021: Dose IQ Safety Software used with Spectrum IQ Infusion Pump
FDA device recall · Class I · Baxter Healthcare Corporation
Key facts
| Recall number (Z-number) | Z-2165-2021 |
|---|---|
| Recall event | 88246 |
| Product | Dose IQ Safety Software used with Spectrum IQ Infusion Pump |
| Product code | FRN |
| Recalling firm | Baxter Healthcare Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 20, 2024 |
| 510(k) numbers | K173084 |
| FEI number | 1417572 |
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