Device recall
Z-0460-2026: Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03…
FDA device recall · Class II · Sonesta Medical AB
Key facts
| Recall number (Z-number) | Z-0460-2026 |
|---|---|
| Recall event | 97568 |
| Product | Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Version: N/A Product Description: Sonesta 6210 - Procedure table designed for full fluoroscopic imaging of the urinary tract during video Urodynamics procedures. Component: N/A |
| Product code | IXR |
| Recalling firm | Sonesta Medical AB |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3010496070 |
At a glance
- None 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