Deserving Health Symbio Muc Eye Eye Drops Recall: Lack of Sterility Assurance
Deserving Health recalls Symbio Muc Eye eye drops due to lack of sterility assurance. Products manufactured for US distribution may pose infection risks. Consumers should contact the manufacturer for details.
Recall notice
Lack of Assurance of Sterility
Contact the company
What happened, in plain English
Deserving Health is recalling Symbio Muc Eye eye drops because they may not be sterile. Using these products could lead to infections, especially if someone has a compromised immune system or open wounds. Read more at govinfonow.com/recall/41245-deserving-health-symbio-muc-eye-eye-drops-recall-lack-of.
Source Summary by GovInfoNow · govinfonow.com/recall/41245-deserving-health-symbio-muc-eye-eye-drops-recall-lack-of · Updated October 7, 2026 · FDA enforcement record: FDA #D-0011-2018
Cite this page
“Deserving Health Symbio Muc Eye Eye Drops Recall: Lack of Sterility Assurance.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41245-deserving-health-symbio-muc-eye-eye-drops-recall-lack-of. Based on FDA recall #D-0011-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0011-2018%22&limit=1).
Why it’s dangerous
The eye drops may not be sterile, which means they could cause infections. This is particularly dangerous for people with compromised immune systems or open wounds, as their bodies may not fight off infections effectively.
Who’s affected
People who purchased Symbio Muc Eye eye drops in the US between 2019 and 2020 are affected. Those with weakened immune systems or open wounds are at higher risk of infection.
How to tell if you have this one
Check for the product name 'Symbio Muc Eye', 0.17 fl.oz. 5mL bottles, and the lot numbers DM17B12 (expiring 03/2020), DM16L44 (expiring 12/2019), or DM16L07 (expiring 12/2019).
- Brand
Deserving Health- Category
Drug
What to do — step by step
Check Product Details
Look for the lot numbers DM17B12 (expiring 03/2020), DM16L44 (expiring 12/2019), or DM16L07 (expiring 12/2019) on the bottle.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Product was distributed throughout the United States.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 16 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0011-2018 (September 20, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0011-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.