# FDA recall Z-0326-2026

> **Alcon Research LLC** · Class II · device recall initiated 2025-09-30.

## Product

Alcon PRECISION1 One-Day Contact Lenses, -2.25D.

## Reason for recall

Potential for a weak seal in some units resulting in compromise in sterility.

## Distribution

Worldwide - US distribution in the states of Alabama, Arizona, Arkansas, Connecticut, Florida, Idaho, Iowa, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, New Jersey, New York, Oklahoma, Oregon, Tennessee, Texas, Washington and the country of Canada.

## Key facts

- **Recall number:** Z-0326-2026
- **Recalling firm:** Alcon Research LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-30
- **Report date:** 2025-11-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fort Worth, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0326-2026

## Citation

> AI Analytics. FDA recall Z-0326-2026. Retrieved 2026-08-24 from https://api.ai-analytics.org/recall/Z-0326-2026. Source: US FDA. Licensed CC0.

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