Eyebright Concentrate Topical Eye Rinse — Class II drug recall D-912-2013
Terminated recall by Earthlabs, Inc. DBA Wise Woman Herbals, reported 2013-08-28, distributed nationwide. Lack of Assurance of Sterility; Lack of Assurance of Sterility; product not manufactured under sterile conditi
| Recall number | D-912-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Earthlabs, Inc. DBA Wise Woman Herbals, Creswell, OR, United States |
| Recall initiated | 2013-05-27 |
| Classified | 2013-08-20 |
| Reported by FDA | 2013-08-28 |
| Terminated | 2013-11-21 |
| Distributed | Nationwide (US) |
| Quantity | 581 x |
| Reason classes | sterility |
| Lot numbers | 10010, 10285, 10640, 11107, 11408, 11711, 12088 |
Product
Eyebright Concentrate Topical Eye Rinse, 1, 2, 4, 8, 16 & 32 fl oz bottles, Produced and distributed by: Wise Woman Herbals, Creswell, OR
Reason for recall
Lack of Assurance of Sterility; Lack of Assurance of Sterility; product not manufactured under sterile conditions as required for ophthalmic drug products
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-912-2013. 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.