Device recall
Z-2669-2026: Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI…
FDA device recall · Class II · Laborie Medical Technologies Corp
Key facts
| Recall number (Z-number) | Z-2669-2026 |
|---|---|
| Recall event | 98876 |
| Product | Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar GI HRM H2O, 24p, Compact Pole system (G3-7), Solar GI HRM H2O, 24p, Trolley system (G3-8), Solar GI HRM H2O, 36p, Trolley system (G3-12), Solar GI HRAM H2O, 24p, Trolley system… |
| Product code | FFX |
| Recalling firm | Laborie Medical Technologies Corp |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K121014 |
| FEI number | 3017448360 |
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