FDA Drug recall D-0011-2018
Symbio Muc Eye, 0.17 fl.oz. 5mL bottles, Manufactured for and distributed in the US b: Biological Health Group Corp
- FDA Drug
- Class II
- terminated
- Published 2017-10-25
On 2017-10-25 the FDA classified a Class II recall of Symbio Muc Eye, 0.17 fl.oz. 5mL bottles, Manufactured for and distributed in the US b: Biological Health Group Corp by Deserving Health International, citing lack of Assurance of Sterility.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0011-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-09-20 |
| Published | 2017-10-25 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Deserving Health International |
| Distribution | US |
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
Lack of Assurance of Sterility
Identifiers
| code_info | Lot #: DM17B12, Exp 03/2020; DM16L44, Exp 12/2019; DM16L07, Exp12/2019 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0011-2018%22
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