Device recall
Z-1805-2009: POWERSAIL Coronary Dilatation Catheter: 4.0x8mm (CE) Part #1005726-08
FDA device recall · Class I · Abbott Vascular-Cardiac Therapies dba Guidant Corporation
Key facts
| Recall number (Z-number) | Z-1805-2009 |
|---|---|
| Recall event | 52705 |
| Product | POWERSAIL Coronary Dilatation Catheter: 4.0x8mm (CE) Part #1005726-08 |
| Product code | MAF |
| Recalling firm | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 6, 2010 |
| PMA numbers | P810046 |
| 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