FDA recall record

Kadesh International puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc. recall — FDA D-0250-2019

Non-Sterility: Product manufactured under non-sterile production conditions.

Class Iclassification
D-0250-2019official record ID
Nov 21, 2018report date

Recall record at a glance

Official recordD-0250-2019
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmKadesh International
Report dateNov 21, 2018
Recall initiation dateNov 5, 2018
Quantity18,521 bottles
LocationGarden Grove, CA, United States

Official product description

puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.

Why the product was recalled

Non-Sterility: Product manufactured under non-sterile production conditions.

Distribution information

Product was distributed via online stores and retail distributors Nationwide in the USA, Uruguay, Canada, China, Dominican Republic, Korea, and Vietnam.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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