Device recall
Z-0896-2010: Electri-Cord Manufacturing Corporation (312 E. Main St., Westfield, PA 16950) AC…
FDA device recall · Class II · Arizant Inc
Key facts
| Recall number (Z-number) | Z-0896-2010 |
|---|---|
| Recall event | 54487 |
| Product | Electri-Cord Manufacturing Corporation (312 E. Main St., Westfield, PA 16950) AC power cords used with Ranger Blood/Fluid Warming Unit: Model 245. Intended to warm blood, blood products and liquids. |
| Product code | DWJ |
| Recalling firm | Arizant Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2012 |
| 510(k) numbers | K053645 |
| FEI number | 2183725 |
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