# FDA recall Z-1014-2023

> **CooperVision, Inc.** · Class II · device recall initiated 2022-12-27.

## Product

MyDay Toric (90-pack)  Reveal 1 Day Toric (90-pack)    Soft (hydrophilic) Contact Lens (daily wear). Single Use.

## Reason for recall

Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.

## Distribution

Distribution to US states of CA, FL, IA, KY, NC, NY, OH, OR, WI; Canada and Japan.

## Key facts

- **Recall number:** Z-1014-2023
- **Recalling firm:** CooperVision, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-27
- **Report date:** 2023-02-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Henrietta, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1014-2023

## Citation

> AI Analytics. FDA recall Z-1014-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1014-2023. Source: US FDA. Licensed CC0.

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