Medical DeviceOct 1, 2025
CooperVision MyDay Toric, stenfilcon A) Contact Lens recall — FDA Z-2606-2025
One lot manufactured with an invalid sterilization cycle.
Class IIFDA: OngoingCooperVision, Inc.
Recall history in this database
Classification mix: Class II: 20, Class III: 5.
Medical DeviceOct 1, 2025
CooperVision Voyant 1-Day Premium Toric, (stenfilcon A) contact lens recall — FDA Z-2608-2025
One lot manufactured with an invalid sterilization cycle.
Class IIFDA: OngoingCooperVision, Inc.
Medical DeviceOct 1, 2025
CooperVision Sofmed Breathables, (stenfilcon A) contact lens recall — FDA Z-2607-2025
One lot manufactured with an invalid sterilization cycle.
Class IIFDA: OngoingCooperVision, Inc.
Medical DeviceApr 2, 2025
CooperVision (Stenfilcon A) Contact Lens recall — FDA Z-1455-2025
a limited number of lots were manufactured with an incorrect cylinder power.
Class IIFDA: OngoingCooperVision, Inc.
Medical DeviceOct 9, 2024
CooperVision Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the recall — FDA Z-3311-2024
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
Class IIFDA: OngoingCooperVision, Inc.
Medical DeviceOct 9, 2024
CooperVision BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of recall — FDA Z-3310-2024
Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
Class IIFDA: OngoingCooperVision, Inc.
Medical DeviceMar 29, 2023
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 IIFDA: OngoingCooperVision, Inc.
Medical DeviceFeb 1, 2023
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 IIFDA: OngoingCooperVision, Inc.
Medical DeviceAug 4, 2021
CooperVision SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens recall — FDA Z-2148-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens recall — FDA Z-2144-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with recall — FDA Z-2153-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with recall — FDA Z-2150-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with recall — FDA Z-2146-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with recall — FDA Z-2147-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable Contact recall — FDA Z-2149-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens recall — FDA Z-2151-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with recall — FDA Z-2152-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact recall — FDA Z-2154-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with recall — FDA Z-2145-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceAug 4, 2021
CooperVision CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with recall — FDA Z-2143-2021
Misaligned placement of an axis mark can cause the patient to experience blurred vision
Class IIFDA: TerminatedCooperVision Inc.
Medical DeviceMay 2, 2018
CooperVision clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily recall — FDA Z-1516-2018
The secondary packaging is labeled with an incorrect expiration date.
Class IIIFDA: TerminatedCooperVision Inc.
Medical DeviceMay 2, 2018
CooperVision 56% 1 Day Silicone Hydrogel (-4.50), 10 pack, UV Blocking, daily disposable recall — FDA Z-1517-2018
The secondary packaging is labeled with an incorrect expiration date.
Class IIIFDA: TerminatedCooperVision Inc.
Medical DeviceMay 2, 2018
CooperVision clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel recall — FDA Z-1515-2018
The secondary packaging is labeled with an incorrect expiration date.
Class IIIFDA: TerminatedCooperVision Inc.
Medical DeviceMay 2, 2018
CooperVision 56% 1 Day Silicone Hydrogel (-2.50), 10 pack, UV Blocking, daily disposable recall — FDA Z-1518-2018
The secondary packaging is labeled with an incorrect expiration date.
Class IIIFDA: TerminatedCooperVision Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies CooperVision, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.