Device recall
Z-2275-2026: PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
FDA device recall · Class II · Oculus Technologies of Mexico, S.A. de C.V.
Key facts
| Recall number (Z-number) | Z-2275-2026 |
|---|---|
| Recall event | 98959 |
| Product | PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050 |
| Product code | FRO |
| Recalling firm | Oculus Technologies of Mexico, S.A. de C.V. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K172851 |
| FEI number | 3007244484 |
At a glance
- 1–9 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