DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | March 25, 2026 |
| Reported | May 13, 2026 |
| Recalling firm | Katalyst Surgical, LLC |
| Country / region | United States MO |
Hazard
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Affected products
- DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
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