Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
puriton EYE RELIEF DROPS Recalled by Kadesh International Due to Non-Sterility: Product manufactured under non-sterile production conditions.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Kadesh International directly.
Affected Products
puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.
Quantity: 18,521 bottles
Why Was This Recalled?
Non-Sterility: Product manufactured under non-sterile production conditions.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Kadesh International
Kadesh International has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report