Device recall
Z-0983-03: CP STENT (Cheatham Platinum), a prescription device, composed of 90%…
FDA device recall · Class II · Numed Inc
Key facts
| Recall number (Z-number) | Z-0983-03 |
|---|---|
| Recall event | 26556 |
| Product | CP STENT (Cheatham Platinum), a prescription device, composed of 90% platinum/10% iridium wire arranged in laser welded rows with a ''zig'' pattern. The number of zigs can be varied and will impact the strength of the stent as well as the eventual diameter and percent stent shortening. CP stents are… |
| Product code | MAF |
| Recalling firm | Numed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 9, 2004 |
| FEI number | 1318694 |
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