Kadesh International is recalling approximately 18,521 bottles of puriton EYE RELIEF DROPS (0.5 oz / 15 ml). These eye drops were manufactured under non-sterile production conditions, which is a critical safety failure for products intended for use in the eyes. The affected products were sold nationwide through online stores and various retail distributors. Consumers should stop using these eye drops immediately and contact their healthcare provider or pharmacist for guidance, then return the product to the place of purchase for a full refund.
Products used in the eyes must be sterile; because these drops were made in a non-sterile environment, they pose a serious risk of causing eye infections or other vision-threatening injuries.
Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund and contact the manufacturer for further instructions.
Box Label, Puriton Eye Relief Drops
Image 2 - Label, Puriton Eye Relief Drops
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · FDA Press Release (1) · FDA Press Release (2) · Raw API Response
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