Device recall
Z-0570-2026: Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30…
FDA device recall · Class I · Olympus Corporation of the Americas
Key facts
| Recall number (Z-number) | Z-0570-2026 |
|---|---|
| Recall event | 97731 |
| Product | Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog Number: HX-400U-30 Used with an Olympus endoscope to deliver a nylon loop snare. |
| Product code | MND |
| Recalling firm | Olympus Corporation of the Americas |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 2429304 |
At a glance
- None 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