Device recall
Z-0775-03: Guidant Multi-Link Vision Coronary Stent System Catalog Numbers: 30 different…
FDA device recall · Class II · Guidant Corporation ACS
Key facts
| Recall number (Z-number) | Z-0775-03 |
|---|---|
| Recall event | 25945 |
| Product | Guidant Multi-Link Vision Coronary Stent System Catalog Numbers: 30 different catalog numbers have been listed. The firm indicates that total numbers of devices subject to this removal are being defined. |
| Recalling firm | Guidant Corporation ACS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2004 |
| PMA numbers | P020047 |
| FEI number | 2024168 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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