Device recall
Z-1075-03: Guidant Multi-Link Zeta Coronary Stent System
FDA device recall · Class II · Guidant Corporation ACS
Key facts
| Recall number (Z-number) | Z-1075-03 |
|---|---|
| Recall event | 26836 |
| Product | Guidant Multi-Link Zeta Coronary Stent System |
| Recalling firm | Guidant Corporation ACS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2004 |
| PMA numbers | P970020, P970020S042 |
| 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