Device recall
Z-2080-2026: DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog…
FDA device recall · Class II · Katalyst Surgical, LLC
Key facts
| Recall number (Z-number) | Z-2080-2026 |
|---|---|
| Recall event | 98660 |
| Product | DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27 |
| Product code | HNR |
| Recalling firm | Katalyst Surgical, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3007589150 |
At a glance
- None Linked 510(k)s
- 10–99 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