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Kadesh recalls Puriton Eye Relief Drops

The product was manufactured without necessary production controls and conditions to assure sterility

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Photo source: FDA
Kadesh, Inc., of Garden Grove, Calif., is recalling all lots of Puriton Eye Relief Drops.

The product was manufactured without necessary production controls and conditions to assure sterility.

There are no reports of adverse events related to this recall.

The recalled product, an over-the-counter homeopathic eye drop for the temporary relief of burning and irritation due to dryness of the eye packaged in a 15-ml plastic bottle, NDC 7079600115, UPC 7 36972 1679 0, was sold nationwide through the company’s online stores and retail distributors.

What to do

Kadesh is notifying its customers by recall letter and arranging for the return of all recall products.

Customers who purchased the recalled product should stop using it.

Consumers with questions may contact the recall department at by email at contact@puriton.us Monday through Friday, from 9 am – 6 pm (Pacific Time).

The recalled product may be returned to Kadesh Inc., 4731 Lincoln Way, Garden Grove, CA 92841.

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