Eye Wash — Class II drug recall D-0498-2017
Terminated recall by United Exchange Corporation, reported 2017-03-08, distributed nationwide. Lack of assurance of sterility
| Recall number | D-0498-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | United Exchange Corporation, Cerritos, CA, United States |
| Recall initiated | 2016-09-02 |
| Classified | 2017-02-27 |
| Reported by FDA | 2017-03-08 |
| Terminated | 2017-06-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | GY |
| Quantity | 77,184 bottles |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00780707005828 |
| Lot numbers | G15901, G15902, G15903, G15904, G16909 |
| Expiration dates | 2018-07-31, 2019-05-30 |
Product
Eye Wash, 4 fl oz (118 mL) bottle, OTC, Distributed by: United Exchange Corp., 17211 Valley View Ave., Cerritos, CA 90703, Made in Korea, UPC Code: 780707005828
Reason for recall
Lack of assurance of sterility
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-0498-2017. 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.