Device recall
Z-1512-2025: Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration…
FDA device recall · Class I · Qapel Medical Inc.
Key facts
| Recall number (Z-number) | Z-1512-2025 |
|---|---|
| Recall event | 96492 |
| Product | Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072 Aspiration System including Cheetah Delivery Tool, REF: AP6072-132. 072 Aspiration Tubing, REF: APT-95 |
| Product code | NRY |
| Recalling firm | Qapel Medical Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K222786 |
| FEI number | 3020954126 |
At a glance
- 1–9 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