EPA (Environmental Protection Agency)
1 records
fda
23 records
FDA Device Recall: MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 5
2025-10-01
Class II — One lot manufactured with an invalid sterilization cycle.
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FDA Device Recall: Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-
2025-10-01
Class II — One lot manufactured with an invalid sterilization cycle.
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FDA Device Recall: Biofinity XR Toric Contact Lens
2025-07-30
Class II — Lens blisters may have an incomplete or leaking seal which may render them unsterile.
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FDA Device Recall: Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correc
2024-10-09
Class II — Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
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FDA Device Recall: BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for the correction of
2024-10-09
Class II — Manufactured with a misaligned axis resulting in lenses with the incorrect power, may experience poor visual acuity
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FDA Recall: CooperVision, Inc. — Class II
20230308
Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity | Product: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended...
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FDA Device Recall: Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
2023-03-29
Class II — The lenses manufactured in the affected lot were made with a misaligned axis resulting in lenses with the incorrect power.
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FDA Device Recall: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)
2023-03-08
Class II — Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
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FDA Device Recall: Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens (exte
2023-03-08
Class II — Manufactured with misaligned axis resulting in lenses with the incorrect power, users may experience poor visual acuity
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FDA Device Recall: SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens
2021-08-04
Class II — Misaligned placement of an axis mark can cause the patient to experience blurred vision
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FDA Device Recall: AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Le
2021-08-04
Class II — Misaligned placement of an axis mark can cause the patient to experience blurred vision
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FDA Device Recall: FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens
2021-08-04
Class II — Misaligned placement of an axis mark can cause the patient to experience blurred vision
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FDA Device Recall: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens w
2021-08-04
Class II — Misaligned placement of an axis mark can cause the patient to experience blurred vision
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FDA Device Recall: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens wit
2021-08-04
Class II — Misaligned placement of an axis mark can cause the patient to experience blurred vision
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FDA Device Recall: CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens wi
2021-08-04
Class II — Misaligned placement of an axis mark can cause the patient to experience blurred vision
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FDA Recall: CooperVision Inc. — Class II
20200219
Incorrect power of lenses than the expected | Product: Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (e
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FDA Device Recall: Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophi
2020-02-19
Class II — Incorrect power of lenses than the expected
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FDA Device Recall: Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophi
2020-02-19
Class II — Incorrect power of lenses than the expected
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FDA Recall: CooperVision Inc. — Class III
20180502
The secondary packaging is labeled with an incorrect expiration date. | Product: clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily disposable contact lenses
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FDA Device Recall: clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily disposab
2018-05-02
Class III — The secondary packaging is labeled with an incorrect expiration date.
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FDA Device Recall: Biofinity XR Toric contact lenses 8.7/14.5 - 6PK Biofinity XR Toric (comfil
2018-03-07
Class III — 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 Bio...
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FDA Device Recall: Pro clear(R) 1 day Sphere (o mafilcon A), 90 daily disposable contact lenses, ST
2013-12-25
Class II — Lots were labeled with incorrect expiration dates on secondary package (carton). The primary package (blister) is marked with the correct expiration date.
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FDA Device Recall: ClearSight(TM) Toric 1 day (ocufilcon D), 30 daily disposable contact lenses for
2013-12-25
Class II — Lots were labeled with incorrect expiration dates on secondary package (carton). The primary package (blister) is marked with the correct expiration date.
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ny_corps
1 records
NY Corp: COOPERVISION, INC.
1959-02-20
DOMESTIC BUSINESS CORPORATION | County: Monroe | Jurisdiction: New York
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