Device recall
Z-2451-2025: Akreos, SKU: AO60P0300. Akreos intraocular lenses
FDA device recall · Class III · Bausch & Lomb Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-2451-2025 |
|---|---|
| Recall event | 97232 |
| Product | Akreos, SKU: AO60P0300. Akreos intraocular lenses |
| Product code | HQL |
| Recalling firm | Bausch & Lomb Surgical, Inc. |
| Recall class | Class III |
| Status | Open, Classified |
| PMA numbers | P060022 |
| FEI number | 1119279 |
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