Clerio Vision Contact Lenses Recalled for Incorrect Power Labeling
Clerio Vision is recalling one lot of contact lenses because the packaging labeled them as -2.25 power, but the lenses inside are -3.75 power.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the hazard is a labeling error (incorrect power) rather than a contamination or structural defect. No injuries or illnesses are reported in the source text, fitting the criteria for moderate severity involving labeling errors.
Plain-English summary
Clerio Vision is recalling one lot of contact lenses due to a labeling error. The product is identified as 'Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25' with UPC 675506803334 (6 count) and UPC 675506804478 (12 count). The specific lot number is 3100246509, with an expiration date of 2026/09.
The recall was initiated because the contact lenses contained in the packaging were found to be -3.75 power, despite the label indicating -2.25 power. This discrepancy means the lenses do not match the prescription indicated on the box. The total quantity involved is 208 lenses, which were distributed nationwide in the United States.
Consumers who have purchased these specific lenses should stop using them immediately. They should contact Clerio Vision for instructions on how to return the product or obtain a refund. The lenses are indicated for daily wear for the correction of visual acuity in persons with non-diseased eyes.
The recalled product
- Product
- Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and UPC 675506804478 (12 count) - Product Usage: for daily wear is indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or…
- Manufacturer
- Clerio Vision
- Category
- Medical Device — Contact Lenses
- Hazard
- Affected units
- 208
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- LOT 3100246509
- EXP 2026/09
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · Clerio Vision
See all →- ModerateClerio Vision Recalls Extreme H2O 59% Contact Lenses for Mislabeled Power
FDA (Devices) · 2021-04-14
Same hazard · mis labeling
See all →- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-10-14
- SevereBetter Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- ModerateHalyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
FDA (Devices) · 2026-10-14
Similar recalls
- ModerateClerio Vision Recalls Extreme H2O 59% Contact Lenses for Mislabeled Power
FDA (Devices) · 2021-04-14
- ModerateCooperVision Vertex Toric Contact Lenses Recalled for Incorrect Power
FDA (Devices) · 2020-02-19
- HighContact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision
FDA (Devices) · 2021-08-04
- HighContact lenses for astigmatism recalled due to incorrect cylinder power
FDA (Devices) · 2025-04-02
- HighContact lens recall due to misaligned axis marking
FDA (Devices) · 2021-08-04
- ModerateAMO TECNIS CL Intraocular Lenses Recalled for Incorrect Diopter Power Labeling
FDA (Devices) · 2014-08-27