Device recall
Z-0895-2010: 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-0895-2010 |
|---|---|
| Recall event | 54487 |
| Product | Electri-Cord Manufacturing Corporation (312 E. Main St., Westfield, PA 16950) AC power cords used with either Bair Paws Temperature Management Units: Models 850 and 875 Bair Hugger Temperature Management Units: Models 500/OR, 505, 750 and 775 Indicated for hyper- or hypothermic patients or… |
| 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