Device recall
Z-0677-2025: DiaSorin LIAISON Q.S.E.T. Device Plus, REF 319060; intended for use in the…
FDA device recall · Class II · Diasorin Inc.
Key facts
| Recall number (Z-number) | Z-0677-2025 |
|---|---|
| Recall event | 95829 |
| Product | DiaSorin LIAISON Q.S.E.T. Device Plus, REF 319060; intended for use in the preparation of human stool specimens |
| Product code | NXO |
| Recalling firm | Diasorin Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K213858 |
| FEI number | 2182595 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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