# FDA recall Z-2075-2026

> **Katalyst Surgical, LLC** · Class II · device recall initiated 2026-03-25.

## Product

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-S

## Reason for recall

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

## Distribution

Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.

## Key facts

- **Recall number:** Z-2075-2026
- **Recalling firm:** Katalyst Surgical, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-25
- **Report date:** 2026-05-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chesterfield, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2075-2026

## Citation

> AI Analytics. FDA recall Z-2075-2026. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2075-2026. Source: US FDA. Licensed CC0.

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