Device recall
Z-0071-04: PeriVac brand Pericardial Fluid Aspiration Procedure Kit (Pericardiocentensis…
FDA device recall · Class II · Boston Scientific
Key facts
| Recall number (Z-number) | Z-0071-04 |
|---|---|
| Recall event | 27454 |
| Product | PeriVac brand Pericardial Fluid Aspiration Procedure Kit (Pericardiocentensis Kit), with Pigtail Drainage Catheter; Model/Catalog Numbers: 4304 and 4305 |
| Product code | DQX |
| Recalling firm | Boston Scientific |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2004 |
| 510(k) numbers | K032050 |
| FEI number | 3001236349 |
At a glance
- 1–9 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