Device recall
Z-1421-2010: Cordis, AVANTI+ Introducer, STERILE EO, For one use only. Catalog 402656X Lot #…
FDA device recall · Class II · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-1421-2010 |
|---|---|
| Recall event | 54547 |
| Product | Cordis, AVANTI+ Introducer, STERILE EO, For one use only. Catalog 402656X Lot # 15076369. Catalog 504606X Lot # 15075717. Catalog 504656X Lot # 15076362, 15076363, 15076364. |
| Product code | DYB |
| Recalling firm | Cordis Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 27, 2012 |
| 510(k) numbers | K945616 |
| FEI number | 1016427 |
At a glance
- 1–9 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