CooperVision Recalls
33 recalls on record · December 25, 2013 to October 1, 2025 · Medical Devices
Recalls by year
13
18
20
21
23
24
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 1, 2025Medical DevicesFDA
CooperVision, Inc. recalls Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content,
Hazard: One lot manufactured with an invalid sterilization cycle.
October 1, 2025Medical DevicesFDA
CooperVision, Inc. recalls Sofmed Breathables, (stenfilcon A) contact lens. Model Number: Softmed Breathables. 54% water content, Toric, cast mo
Hazard: One lot manufactured with an invalid sterilization cycle.
October 1, 2025Medical DevicesFDA
CooperVision, Inc. recalls MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Si
Hazard: One lot manufactured with an invalid sterilization cycle.
July 30, 2025Medical DevicesFDA
CooperVision, Inc. recalls Biofinity Toric Multifocal Contact Lens
Hazard: Lens blisters may have an incomplete or leaking seal which may render them unsterile.
July 30, 2025Medical DevicesFDA
CooperVision, Inc. recalls Biofinity XR Toric Contact Lens
Hazard: Lens blisters may have an incomplete or leaking seal which may render them unsterile.
April 2, 2025Medical DevicesFDA
CooperVision, Inc. recalls Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1
Hazard: a limited number of lots were manufactured with an incorrect cylinder power.
October 9, 2024Medical DevicesFDA
CooperVision, Inc. recalls Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia w
Hazard: Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
October 9, 2024Medical DevicesFDA
CooperVision, Inc. recalls BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia with asti
Hazard: Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
March 29, 2023Medical DevicesFDA
CooperVision, Inc. recalls Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
Hazard: The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
March 8, 2023Medical DevicesFDA
CooperVision, Inc. recalls Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens (extended wear)
Hazard: Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
March 8, 2023Medical DevicesFDA
CooperVision, Inc. recalls Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)
Hazard: Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
February 1, 2023Medical DevicesFDA
CooperVision, Inc. recalls MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.
Hazard: Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
August 4, 2021Medical DevicesFDA
CooperVision Inc. recalls CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Hazard: Misaligned placement of an axis mark can cause the patient to experience blurred vision
February 19, 2020Medical DevicesFDA
CooperVision Inc. recalls Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear)
Hazard: Incorrect power of lenses than the expected
February 19, 2020Medical DevicesFDA
CooperVision Inc. recalls Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)
Hazard: Incorrect power of lenses than the expected
May 2, 2018Medical DevicesFDA
CooperVision Inc. recalls 56% 1 Day Silicone Hydrogel (-2.50), 10 pack, UV Blocking, daily disposable contact lenses The Clariti 1 Day (somof
Hazard: The secondary packaging is labeled with an incorrect expiration date.
May 2, 2018Medical DevicesFDA
CooperVision Inc. recalls 56% 1 Day Silicone Hydrogel (-4.50), 10 pack, UV Blocking, daily disposable contact lenses The Clariti 1 Day (somof
Hazard: The secondary packaging is labeled with an incorrect expiration date.
May 2, 2018Medical DevicesFDA
CooperVision Inc. recalls clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily disposable contact lenses The Clariti 1 Day
Hazard: The secondary packaging is labeled with an incorrect expiration date.
May 2, 2018Medical DevicesFDA
CooperVision Inc. recalls clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clari
Hazard: The secondary packaging is labeled with an incorrect expiration date.