puriton EYE RELIEF DROPS — Class I drug recall D-0250-2019
Terminated recall by Kadesh International, reported 2018-11-21, distributed nationwide. Non-Sterility: Product manufactured under non-sterile production conditions.
| Recall number | D-0250-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Kadesh International, Garden Grove, CA, United States |
| Recall initiated | 2018-11-05 |
| Classified | 2018-11-19 |
| Reported by FDA | 2018-11-21 |
| Terminated | 2023-01-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, DO, KR, UY, VN |
| Quantity | 18,521 bottles |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00736972167990 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0250-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.