Class IIOngoingZ-2606-2025
CooperVision, Inc. recalls MyDay Toric
One lot manufactured with an invalid sterilization cycle.
- (Disposable) Contact Lens
- Under Investigation by firm
CooperVision, Inc.NYOct 1, 2025
CooperVision, Inc. recalls
The FDA has posted 6 enforcement recalls from CooperVision, Inc. since 2025, none of them Class I (most serious). Most recent report: Oct 1, 2025.
Class II: 6
Latest recalls
View all 6 in the recall browser →Class IIOngoingZ-2608-2025
CooperVision, Inc. recalls Voyant 1-Day Premium Toric
One lot manufactured with an invalid sterilization cycle.
- (Disposable) Contact Lens
- Under Investigation by firm
CooperVision, Inc.NYOct 1, 2025
Class IIOngoingZ-2607-2025
CooperVision, Inc. recalls Sofmed Breathables
One lot manufactured with an invalid sterilization cycle.
- (Disposable) Contact Lens
- Under Investigation by firm
CooperVision, Inc.NYOct 1, 2025
Class IIOngoingZ-2165-2025
CooperVision, Inc. recalls Biofinity XR Toric Contact Lens
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
- Extended Wear Soft Contact Lenses
- Use error
CooperVision, Inc.NYJul 30, 2025
Class IIOngoingZ-2166-2025
CooperVision, Inc. recalls Biofinity Toric Multifocal Contact Lens
Lens blisters may have an incomplete or leaking seal which may render them unsterile.
- Extended Wear Soft Contact Lenses
- Use error
CooperVision, Inc.NYJul 30, 2025
Class IIOngoingZ-1455-2025
CooperVision, Inc. recalls Brand Names: MyDay Toric
a limited number of lots were manufactured with an incorrect cylinder power.
- (Disposable) Contact Lens
- Process control
CooperVision, Inc.NYApr 2, 2025
Firm name as filed with the FDA: “CooperVision, Inc.”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.