CooperVision, Inc. recalls
Every recall we track for CooperVision, Inc. — 32 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from CooperVision, Inc. more than tripled in 2025 (6, up from 2 in 2024).
All FDA recall records for CooperVision, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 4 | 0 | 4 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 1 | 0 | 2 |
| 2021 | 0 | 0 | 12 | 0 | 12 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 3 | 0 | 3 |
| 2024 | 0 | 1 | 1 | 0 | 2 |
| 2025 | 0 | 0 | 5 | 1 | 6 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
Most common reasons for CooperVision, Inc. recalls
What to do if you have a recalled CooperVision, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All CooperVision, Inc. recalls
12 shown- Lower riskMedical device
CooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
CooperVision recalls Pearle Vision 1 day contact lenses with incorrect power in some lots. Affected lenses may not provide proper vision correction. Consumers should check carton and blister lot numbers for affected items.
CooperVisionAug 12, 2026 - UnratedMedical device
CooperVision, Inc. recalls MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded
CooperVision recalls MyDay Toric contact lenses made with an invalid sterilization cycle. This could lead to improper lens safety. Affected units include specific lot numbers from 20735504301008 carton.
CooperVisionAug 22, 2025 - Lower riskMedical device
CooperVision, Inc. recalls Biofinity XR Toric Contact Lens
CooperVision recalls Biofinity XR Toric Contact Lenses with specific lot numbers due to potential incomplete seals that could make lenses unsterile. Consumers should check their carton lot numbers to see if they are affected.
CooperVisionJun 16, 2025 - Lower riskMedical device
CooperVision, Inc. recalls Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1
CooperVision recalls limited lots of MyDay Toric contact lenses for astigmatism due to incorrect cylinder power. Consumers should check lot numbers and contact CooperVision for a replacement.
CooperVisionFeb 27, 2025 - Use cautionMedical device
CooperVision, Inc. recalls Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for the correction of ametropia (myopia or hyperopia
CooperVision recalls 2,443 Biofinity Toric Multifocal contact lenses due to misaligned axis causing incorrect power. Check lot numbers RB0444532 through RC1253124.
CooperVisionAug 29, 2024 - Lower riskMedical device
CooperVision, Inc. recalls Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
CooperVision recalls Clariti 1-day toric soft contact lenses with incorrect power due to misaligned axis. Affected lot W0124677.
CooperVisionFeb 14, 2023 - Lower riskMedical device
CooperVision, Inc. recalls Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)
CooperVision recalls Biofinity XR Toric 6-pack soft contact lenses with misaligned axis causing incorrect power. Affected lot numbers: R24377024, R24377: R24377026, R24381716, R24416900.
CooperVisionJan 26, 2023 - Lower riskMedical device
CooperVision, Inc. recalls MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact Lens (daily wear). Single Use.
CooperVision recalls 90-pack MyDay Toric and Reveal : Lenses may have incorrect power causing poor vision. Affected customers should contact for remedy.
CooperVisionDec 27, 2022 - Lower riskMedical device
CooperVision Inc. recalls SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
CooperVision recalls SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lenses with UV blocker due to potential blurred vision from misaligned axis marks. Affected lenses have Lot Number U0108940.
CooperVisionMay 19, 2021 - Use cautionMedical device
CooperVision Inc. recalls Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)
CooperVision is recalling specific lots of Vertex Toric contact lenses because the power may be incorrect. Check your lot numbers immediately.
CooperVisionJan 13, 2020 - Lower riskMedical device
CooperVision Inc. recalls clariti 1 day (-1.25) 90 pack, UV Blocking, 90 silicone hydrogel, daily disposable contact lenses The Clariti 1 Day
CooperVision recalls Clariti 1 Day (-1.25) 90-pack contact lenses due to incorrect expiration date labeling on secondary packaging. Affected units have a foil expiration date of 6/30/2020 and carton expiration date of 6/20/2030.
CooperVisionFeb 21, 2018 - Lower riskMedical device
CooperVision Inc. recalls Biofinity XR Toric contact lenses 8.7/14.5 - 6PK Biofinity XR Toric (comfilcon A) Soft (Hydrophilic) Contact Lenses are
CooperVision recalls Biofinity XR Toric contact lenses with incorrect labeling on Made-To-Order blister packs. The label shows 'Biofinity Multifocal Toric' instead of 'Biofinity XR Toric'. This may cause confusion in prescription use. Affected lots and expiration dates listed.
CooperVisionSep 1, 2017
CooperVision, Inc. recall questions
How many recalls has CooperVision, Inc. had?
32 recalls from CooperVision, Inc. are on record with U.S. safety agencies, from 2017–2026.
What is the most recent CooperVision, Inc. recall?
CooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day, dated Aug 12, 2026. Every CooperVision, Inc. recall is listed on this page, newest first.
Why are CooperVision, Inc. products recalled?
The most common reasons on record: The secondary packaging is labeled with an incorrect expiration date. (4); One lot manufactured with an invalid sterilization cycle. (3); Incorrect power of lenses than the expected (2).
What should I do if I have a recalled CooperVision, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new CooperVision, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.