CooperVision recalls
CooperVision has 33 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 1 Oct 2025. 12 are still ongoing. 3 were reported in the last 12 months.
Total recalls33since 2013
Last 12 months3reported
Class I00% of total
Ongoing12latest 1 Oct 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 28 85%Class III 5 15%
Why coopervision is recalled
Product types
By year
Ongoing coopervision recalls
12 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Sofmed Breathables, (stenfilcon A) contact lens recalled by CooperVision | CooperVision | Mold | Nationwide |
| Device | CLASS II | Voyant 1-Day Premium Toric, (stenfilcon A) contact lens recalled | CooperVision | Mold | Nationwide |
| Device | CLASS II | MyDay Toric, stenfilcon A) Contact Lens recalled by CooperVision | CooperVision | Mold | Nationwide |
| Device | CLASS II | Biofinity Toric Multifocal Contact Lens recalled by CooperVision | CooperVision | Sterility | Nationwide |
| Device | CLASS II | Biofinity XR Toric Contact Lens recalled by CooperVision | CooperVision | Sterility | Nationwide |
| Device | CLASS II | (Stenfilcon A) Contact Lens recalled by CooperVision | CooperVision | Mold | Nationwide |
All coopervision recalls, newest first
33 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.