# FDA recall Z-0411-2026

> **MicroSurgical Technology Inc** · Class II · device recall initiated 2025-08-20.

## Product

MST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48-1000-01

## Reason for recall

An ophthalmic knife has a suction set (not direct patient-contacting), which contains springs contaminated with an unidentified residue that may potentially cause eye irritation

## Distribution

US Nationwide distribution in the state of GA.

## Key facts

- **Recall number:** Z-0411-2026
- **Recalling firm:** MicroSurgical Technology Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-20
- **Report date:** 2025-11-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Redmond, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0411-2026

## Citation

> AI Analytics. FDA recall Z-0411-2026. Retrieved 2026-08-17 from https://api.ai-analytics.org/recall/Z-0411-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
