PlainRecalls
FDA Drug Critical Class I Terminated

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

Reported: November 21, 2018 Initiated: November 5, 2018 #D-0250-2019

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Kadesh International
Units Affected
18,521 bottles
Distribution
Product was distributed via online stores and retail distributors Nationwide in the USA, Uruguay, Canada, China, Dominican Republic, Korea, and Vietnam.
Location
Garden Grove, CA

Frequently Asked Questions

What product was recalled?
puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.. Recalled by Kadesh International. Units affected: 18,521 bottles.
Why was this product recalled?
Non-Sterility: Product manufactured under non-sterile production conditions.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 21, 2018. Severity: Critical. Recall number: D-0250-2019.