Device recall
Z-2653-2024: Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB,2.4 Model/Catalog…
FDA device recall · Class II · Alcon Research LLC
Key facts
| Recall number (Z-number) | Z-2653-2024 |
|---|---|
| Recall event | 94989 |
| Product | Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB,2.4 Model/Catalog Number: 8065772465 Software Version: N/A Product Description: Ophthalmic knife Component: N/A |
| Product code | HNN |
| Recalling firm | Alcon Research LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1610287 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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