Device recall
Z-1183-2007: Arizant Healthcare Ranger Standard Flow Blood/Fluid Warming Disposable Sets with…
FDA device recall · Class II · Arizant Healthcare, Inc
Key facts
| Recall number (Z-number) | Z-1183-2007 |
|---|---|
| Recall event | 38409 |
| Product | Arizant Healthcare Ranger Standard Flow Blood/Fluid Warming Disposable Sets with injection port and extension set, Part Number 24200. For use with a Ranger warming unit. |
| Product code | FPA |
| Recalling firm | Arizant Healthcare, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 2, 2008 |
| 510(k) numbers | K973741 |
| FEI number | 2183725 |
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