Symbio Muc Eye — Class II drug recall D-0011-2018
Terminated recall by Deserving Health International Corp, reported 2017-10-25, distributed nationwide. Lack of Assurance of Sterility
| Recall number | D-0011-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Deserving Health International Corp, Richmond, Canada |
| Recall initiated | 2017-09-20 |
| Classified | 2017-10-18 |
| Reported by FDA | 2017-10-25 |
| Terminated | 2019-01-24 |
| Distributed | Nationwide (US) |
| Quantity | 623 dropper |
| Reason classes | sterility |
| NDC | 69711-0125-61 |
| Lot numbers | DM16L07, DM16L44, DM17B12 |
| Expiration dates | 2019-12, 2020-03 |
Product
Symbio Muc Eye, 0.17 fl.oz. 5mL bottles, Manufactured for and distributed in the US b: Biological Health Group Corp. Bremerton, WA 98337. NDC 69711-125-61
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-0011-2018. 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.