Device recall
Z-1396-05: Aortic Cutter, single use device consisting of grip, cutter, aortic stops…
FDA device recall · Class II · Guidant Cardiac Surgery
Key facts
| Recall number (Z-number) | Z-1396-05 |
|---|---|
| Recall event | 32573 |
| Product | Aortic Cutter, single use device consisting of grip, cutter, aortic stops, needle, safety lock and actuation button. |
| Product code | DYB |
| Recalling firm | Guidant Cardiac Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 9, 2006 |
| FEI number | 3000719698 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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