Device recall
Z-0729-04: Impulse 5F 145 (degree) Multipack Angiographic Catheters, Catalog Number…
FDA device recall · Class II · Boston Scientific Scimed
Key facts
| Recall number (Z-number) | Z-0729-04 |
|---|---|
| Recall event | 28447 |
| Product | Impulse 5F 145 (degree) Multipack Angiographic Catheters, Catalog Number H749163913011 |
| Product code | DQO |
| Recalling firm | Boston Scientific Scimed |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 28, 2006 |
| FEI number | 3002095335 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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