Device recall
Z-1687-2022: Insertion Kit for use with SENSATION PLUS 8F. 50cc Intra-Aortic Balloon Catheter
FDA device recall · Class II · Datascope Corporation
Key facts
| Recall number (Z-number) | Z-1687-2022 |
|---|---|
| Recall event | 90684 |
| Product | Insertion Kit for use with SENSATION PLUS 8F. 50cc Intra-Aortic Balloon Catheter |
| Product code | DSP |
| Recalling firm | Datascope Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K133074 |
| FEI number | 1000222374 |
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