Device recall
Z-0862-03: MULTI-LINK Pixel Coronary Stent System Size: 2.0 x 13 mm OTW Part Number…
FDA device recall · Class II · Guidant Corporation ACS
Key facts
| Recall number (Z-number) | Z-0862-03 |
|---|---|
| Recall event | 26264 |
| Product | MULTI-LINK Pixel Coronary Stent System Size: 2.0 x 13 mm OTW Part Number: 1007830-13 |
| Product code | MAF |
| Recalling firm | Guidant Corporation ACS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 1, 2004 |
| PMA numbers | P970020, P970020S030 |
| FEI number | 2024168 |
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