Professional Formulas Sublinqual B1: Lactose Not Declared on Label
Professional Formulas recalls Sublinqual B12 High-Potency supplements due to lactose in ingredients not listed on label. Affected products include 60-count dissolvable tablets with specific lot numbers and QR codes.
Lower-risk recall
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Contact the company
What happened, in plain English
Professional Formulas is recalling Sublinqual B12 High-Potency dietary supplements because the label does not list milk, even though the ingredients contain lactose. This could cause issues for people with milk allergies or sensitivities. Read more at govinfonow.com/recall/20644-professional-formulas-sublinqual-b1-lactose-not-declared-on-label.
Source Summary by GovInfoNow · govinfonow.com/recall/20644-professional-formulas-sublinqual-b1-lactose-not-declared-on-label · Updated October 7, 2026 · FDA enforcement record: FDA #F-3348-2017
Cite this page
“Professional Formulas Sublinqual B1: Lactose Not Declared on Label.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20644-professional-formulas-sublinqual-b1-lactose-not-declared-on-label. Based on FDA recall #F-3348-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3348-2017%22&limit=1).
Why it’s dangerous
The supplement contains lactose but the label does not declare milk. This means individuals with milk allergies or sensitivities could be exposed to lactose without knowing it's present.
Who’s affected
People who have purchased the recalled Sublinqual B12 supplements are likely affected. Those with milk allergies or sensitivities are at higher risk due to the unlabeled lactose.
How to tell if you have this one
Check for 60-count dissolvable tablets in white plastic bottles with adhesive labels featuring white, black, red, and green print. Lot numbers include 409017, 503019, 508060, 603032, and 701039.
- Brand
Professional Formulas- Category
Food
What to do — step by step
Check Product Label
Look for the label that states the product contains lactose but does not list milk.
Where it went and when
Where it was distributed
Distributed in 34 states, and outside the U.S.
FDA distribution: “distributed in AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MT, NC, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, WA, and WI and in the following countries: Canada and United Kingdom” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Louisiana, Maine, Maryland, Massachusetts, Michigan, Montana, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Washington, Wisconsin.
Recall timeline
FDA terminated this recall 8 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-3348-2017 (July 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3348-2017 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.