Device recall
Z-2380-2010: Vital Signs Inc. enFlow Disposable IV Fluid/Blood Warmer Cartridge. Medical…
FDA device recall · Class II · Vital Signs Inc
Key facts
| Recall number (Z-number) | Z-2380-2010 |
|---|---|
| Recall event | 56561 |
| Product | Vital Signs Inc. enFlow Disposable IV Fluid/Blood Warmer Cartridge. Medical point-of-care device designed to warm blood and IV fluids. |
| Product code | LGZ |
| Recalling firm | Vital Signs Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 27, 2015 |
| 510(k) numbers | K060537 |
| FEI number | 2242551 |
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