CooperVision Recalls

31 recalls on record in the United States

medical: 31
medical Class III
2018-03-07

CooperVision Inc. recalls Biofinity XR Toric contact lenses 8.7/14.5 - 6PK Biofin

The firm identified a labeling error affecting Made-To-Order (MTO) Biofinity XR Toric blister labels. The primary blister reads Biofinity Multifocal Toric in error, and should read Biofinity XR Toric. The outer carton correctly reads Biofinity XR Toric.

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medical Class II
2025-10-01

CooperVision, Inc. recalls MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Numbe

One lot manufactured with an invalid sterilization cycle.

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medical Class II
2025-10-01

CooperVision, Inc. recalls Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Mod

One lot manufactured with an invalid sterilization cycle.

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medical Class II
2025-10-01

CooperVision, Inc. recalls Sofmed Breathables, (stenfilcon A) contact lens. Model Numbe

One lot manufactured with an invalid sterilization cycle.

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medical Class II
2025-07-30

CooperVision, Inc. recalls Biofinity XR Toric Contact Lens

Lens blisters may have an incomplete or leaking seal which may render them unsterile.

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medical Class II
2025-07-30

CooperVision, Inc. recalls Biofinity Toric Multifocal Contact Lens

Lens blisters may have an incomplete or leaking seal which may render them unsterile.

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medical Class II
2025-04-02

CooperVision, Inc. recalls Brand Names: MyDay Toric, LensCrafters One Day Premium Daily

a limited number of lots were manufactured with an incorrect cylinder power.

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medical Class II
2024-10-09

CooperVision, Inc. recalls Biofinity Toric Multifocal Lenses - Soft Contact lenses Indi

Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity

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medical Class II
2024-10-09

CooperVision, Inc. recalls BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated fo

Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity

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medical Class II
2023-03-29

CooperVision, Inc. recalls Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/9

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

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medical Class II
2023-03-08

CooperVision, Inc. recalls Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (

Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity

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medical Class II
2023-03-08

CooperVision, Inc. recalls Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic

Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity

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medical Class II
2023-02-01

CooperVision, Inc. recalls MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft

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

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medical Class II
2021-08-04

CooperVision Inc. recalls SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disp

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily D

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Dis

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Dispo

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposa

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Dispos

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Dai

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Dispo

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 D

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Dispos

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2021-08-04

CooperVision Inc. recalls CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposabl

Misaligned placement of an axis mark can cause the patient to experience blurred vision

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medical Class II
2020-02-19

CooperVision Inc. recalls Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75

Incorrect power of lenses than the expected

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medical Class II
2020-02-19

CooperVision Inc. recalls Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75

Incorrect power of lenses than the expected

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medical Class III
2018-05-02

CooperVision Inc. recalls clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydr

The secondary packaging is labeled with an incorrect expiration date.

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medical Class III
2018-05-02

CooperVision Inc. recalls 56% 1 Day Silicone Hydrogel (-4.50), 10 pack, UV Blocking,

The secondary packaging is labeled with an incorrect expiration date.

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medical Class III
2018-05-02

CooperVision Inc. recalls clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 sil

The secondary packaging is labeled with an incorrect expiration date.

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Showing 30 of 31 recalls. See all →