FDA Device recall Z-1014-2023
MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear)
- FDA Device
- Class II
- ongoing
- Published 2023-02-01
On 2023-02-01 the FDA classified a Class II recall of MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear) by Coopervision, citing lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1014-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-12-27 |
| Published | 2023-02-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Coopervision |
| Distribution | CA, FL, IA, KY, NC, NY, OH, OR, WI |
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.
Identifiers
| code_info | Lot 6474502034 - packaged into 2 packaging lots: 21514501939036, 21514501972036 No UDI |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1014-2023%22
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