Bimatoprost ophthalmic solution
Bimatoprost ophthalmic solution was recalled on 12 July 2019 under EU Safety Gate alert A12/1027/19. Chemical risk reported by Lithuania. According to the label the product contains the active substance bimatoprost, which should be used under supervision of an ophthalmologist.
| Alert Number | A12/1027/19 |
| Brand | Careprost |
| Category | Cosmetics |
| Risk Type | Chemical |
| Notifying Country | Lithuania |
| Country of Origin | India |
| Model Number | 0,03% w/v Sterile Eye drops, 3 ml |
| Published | 12 July 2019 |
Risk Description
According to the label the product contains the active substance bimatoprost, which should be used under supervision of an ophthalmologist. Bimatoprost can cause eye and ophthalmic defects in the user and should not be used by pregnant and breastfeeding women, as it may affect the child.The product does not comply with the Cosmetic Products Regulation.
Measures Taken
Type of economic operator to whom the measure(s) were ordered: RetailerCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: 06/06/2019
Product Description
White plastic bottle with dispenser cap containing ophthalmic solution.
🧪 What Should You Do?
This recall involves a chemical hazard related to Bimatoprost ophthalmic solution.
About this risk
This product contains prohibited or hazardous chemical substances that may cause skin irritation, allergic reactions, or long-term health effects.
Recommended action
Stop using the product immediately. Wash any skin that has come into contact with it. Keep it away from children. Return it to the retailer for a refund if possible.
Who is at risk?
Anyone who has used this product, especially children, pregnant women, and people with sensitive skin.