FDA recall record

CooperVision Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90 recall — FDA Z-1282-2023

The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.

Class IIclassification
Z-1282-2023official record ID
Mar 29, 2023report date

Recall record at a glance

Official recordZ-1282-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCooperVision, Inc.
Report dateMar 29, 2023
Recall initiation dateFeb 14, 2023
Quantity3150
LocationWest Henrietta, NY, United States

Official product description

Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90

Why the product was recalled

The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.

Distribution information

Worldwide - US Nationwide distribution in the states of FL, IL, NY, UT, and WI. The country of Canada.

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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