Device recall
Z-1839-2016: COSEAL Surgical Sealant Kit, 4 mL, Product Code: 934071; For use in vascular…
FDA device recall · Class II · Baxter Healthcare Corp
Key facts
| Recall number (Z-number) | Z-1839-2016 |
|---|---|
| Recall event | 74139 |
| Product | COSEAL Surgical Sealant Kit, 4 mL, Product Code: 934071; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage. |
| Product code | NBE |
| Recalling firm | Baxter Healthcare Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 23, 2017 |
| FEI number | 2937398 |
At a glance
- None 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