US Drug Recall Register
Class I · High risk Terminated Initiated Nov 5, 2018 (8 years ago)

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

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

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

Recalling firm
Kadesh International
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0250-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.