Device recall
Z-0555-05: Cypher Sirolimus-eluting Coronary Stent on Raptor Over-the-Wire Delivery System…
FDA device recall · Class III · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-0555-05 |
|---|---|
| Recall event | 30826 |
| Product | Cypher Sirolimus-eluting Coronary Stent on Raptor Over-the-Wire Delivery System (CWSxxxxx), and Cypher RX Sirolimus-eluting Coronary Stent on RaptorRail Rapid Exchange Delivery System CXSxxxxx |
| Product code | NIQ |
| Recalling firm | Cordis Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 19, 2008 |
| FEI number | 1016427 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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