Device recall
Z-2144-2010: Halobag EVA Dual-Chamber Bag, Sterile R, 3000 mL Total Volume W/500 mL upper…
FDA device recall · Class II · Baxa Corporation
Key facts
| Recall number (Z-number) | Z-2144-2010 |
|---|---|
| Recall event | 55931 |
| Product | Halobag EVA Dual-Chamber Bag, Sterile R, 3000 mL Total Volume W/500 mL upper chamber, Order No. REF: 341, Baxa Corporation. |
| Product code | KPE |
| Recalling firm | Baxa Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2011 |
| 510(k) numbers | K900585 |
| FEI number | 1419106 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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