DEX Ophthalmic Tissue Forceps — Class II medical device recall Z-2069-2026
Ongoing recall by Katalyst Surgical, LLC, reported 2026-05-13, distributed nationwide. Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
| Recall number | Z-2069-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Katalyst Surgical, LLC, Chesterfield, MO, United States |
| Recall initiated | 2026-03-25 |
| Classified | 2026-05-06 |
| Reported by FDA | 2026-05-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, FR, JP, KR, PE |
| Quantity | 5 units |
| UPC / GTIN / UDI-DI | 10817489021658 |
| Lot numbers | M50529 |
| Model numbers | DVF4005-23 |
| Expiration dates | 2028-09-04 |
Product
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
Reason for recall
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2069-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.