FDA recall record

CooperVision MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact recall — FDA Z-1014-2023

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

Class IIclassification
Z-1014-2023official record ID
Feb 1, 2023report date

Recall record at a glance

Official recordZ-1014-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCooperVision, Inc.
Report dateFeb 1, 2023
Recall initiation dateDec 27, 2022
Quantity6,570 lenses
LocationWest Henrietta, NY, United States

Official product description

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

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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