Recall archive / 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. Source coverage and dates.
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
What the recall classes mean. 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.
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.