Eyewash Purified water 98 — Class II drug recall D-1049-2018
Terminated recall by Longbow First Aid Products Manufactory, reported 2018-08-15, distributed in CA, NY. CGMP Deviations
| Recall number | D-1049-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Longbow First Aid Products Manufactory, Foshan, N/A, China |
| Recall initiated | 2018-07-17 |
| Classified | 2018-08-08 |
| Reported by FDA | 2018-08-15 |
| Terminated | 2019-09-11 |
| Distributed | CA, NY |
| Quantity | 14,400 bottles |
| Reason classes | cgmp |
| NDC | 06910-3218-07, 06910-3218-08 |
Product
Eyewash Purified water 98.3%, Ophthalmic Solution, packaged in a) 4 FL OZ (NDC 6910-3218-07) and b) 8 Fl OZ (NDC 6910-3218-08) bottles, 77656 Flora Rd, Palm Desert, CA 92211.
Reason for recall
CGMP Deviations
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-1049-2018. 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.