Device recall
Z-0087-2010: Cordis CROSSOVER. Cordis CROSSOVER Sheath Introducer. Thomas Medical Products…
FDA device recall · Class I · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-0087-2010 |
|---|---|
| Recall event | 53574 |
| Product | Cordis CROSSOVER. Cordis CROSSOVER Sheath Introducer. Thomas Medical Products, Inc. 65 Great Valley Parkway, Malvern, PA 19355 USA. Distributed by Cordis Corporation, 14201 North West 60th Avenue, Miami Lakes, Florida 33014 USA Vital Signs, Ltd. 13-14 Eldon Way Lineside Industrial Estate… |
| Product code | DYB |
| Recalling firm | Cordis Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 12, 2013 |
| 510(k) numbers | K083269 |
| 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