Class II — CooperVision, Inc.
| Recalling firm | COOPERVISION, INC. |
|---|---|
| Registered facility | View this company's 14 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity. |
| Product | MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use. |
| Quantity | 6,570 lenses |
| Distribution | Distribution to US states of CA, FL, IA, KY, NC, NY, OH, OR, WI; Canada and Japan. |
| Initiated | 2022-12-27 |
| Classified | 2023-01-24 |
| Recall number | Z-1014-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — CooperVision, Inc. (Z-1014-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91389/
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