---
title: "MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact... — FDA record Z-1014-2023 | Is It on Recall"
description: "Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity."
url: https://isitonrecall.com/recall/fda-device-z-1014-2023-myday-toric-90-pack-reveal-1-day-toric-90-pack-soft-hydrophilic-contact-lens-daily-wear-single-use/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use. — FDA record Z-1014-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 27, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.
- **Reason**: Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
- **Classification**: Class II
- **Recalling firm**: CooperVision, Inc.
- **Quantity**: 6,570 lenses
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1014-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1014-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot 6474502034 - packaged into 2 packaging lots: 21514501939036, 21514501972036 No UDI |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Iowa](https://isitonrecall.com/state/iowa/)
- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Feb 1, 2023
- **Recall initiation date**: Dec 27, 2022
- **Center classification date**: Jan 24, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1014-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [CooperVision, Inc. records](https://isitonrecall.com/brand/coopervision-inc/)