Garden Grove, CA, United States
Kadesh International recalls
1 recall recorded since 2018, most recently on 5 November 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)1
Terminated Class I Drugs
- Recall started
- 5 November 2018
- Terminated
- 24 January 2023
- Reason
- Non-Sterility: Product manufactured under non-sterile production conditions.
- Distribution
- Product was distributed via online stores and retail distributors Nationwide in the USA, Uruguay, Canada, China, Dominican Republic, Korea, and Vietnam.
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0250-2019
- puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.