Pro Bioteks Bio35 Dietary Supplement Recall: Undeclared Soy Lecithin
Pro Bioteks recalls Bio35 dietary supplement due to undeclared soy lecithin. Consumers should check product details and contact the company for guidance.
Lower-risk recall
Bio-35 has undeclared soy lecithin.
Contact the company
What happened, in plain English
Pro Bioteks is recalling Bio35 dietary supplements because they contain undeclared soy lecithin. This could pose a risk for people with soy allergies or dietary restrictions. The recall affects specific lot numbers and UPC codes. Read more at govinfonow.com/recall/20428-pro-bioteks-bio35-dietary-supplement-recall-undeclared-soy-lecithin.
Source Summary by GovInfoNow · govinfonow.com/recall/20428-pro-bioteks-bio35-dietary-supplement-recall-undeclared-soy-lecithin · Updated October 7, 2026 · FDA enforcement record: FDA #F-0009-2018
Cite this page
“Pro Bioteks Bio35 Dietary Supplement Recall: Undeclared Soy Lecithin.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20428-pro-bioteks-bio35-dietary-supplement-recall-undeclared-soy-lecithin. Based on FDA recall #F-0009-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0009-2018%22&limit=1).
Why it’s dangerous
The supplement contains soy lecithin without being declared on the label. This can cause allergic reactions in people who are sensitive to soy. The undeclared ingredient may also lead to dietary concerns for those following specific diets.
Who’s affected
People who have purchased Bio35 supplements with the specific UPC 0-26341-12900-2 and lot number 2037055 (expiring June 12, 2020) are affected. Those with soy allergies or dietary restrictions are at higher risk.
How to tell if you have this one
Check for the UPC 0-26341-12900-2 and lot number 2037055 on the product label. The supplement expires June 12, 2020.
- Brand
Pro Bioteks- Product
Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Supplement, 100 Softgel Capsules. UPC 0-26341-12900-2- Category
Food
What to do — step by step
Check Product Details
Look for the UPC 0-26341-12900-2 and lot number 2037055 on the product label.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 15 states.
FDA distribution: “Nationwide to AZ, CA, CO, FL, ID, LA, Ml, MN, MO, NM, NV, OR, TX, UT, WA, WY. No foreign/VA/govt/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Colorado, Florida, Idaho, Louisiana, Minnesota, Missouri, Nevada, New Mexico, Oregon, Texas, Utah, Washington, Wyoming.
Recall timeline
FDA terminated this recall 3 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 #F-0009-2018 (September 15, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0009-2018 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.