Device recall
Z-0960-2022: HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10…
FDA device recall · Class II · Huntleigh Healthcare Ltd.
Key facts
| Recall number (Z-number) | Z-0960-2022 |
|---|---|
| Recall event | 89580 |
| Product | HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8 |
| Product code | ITX |
| Recalling firm | Huntleigh Healthcare Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 12, 2024 |
| 510(k) numbers | K201425 |
| FEI number | 1000589001 |
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