GNC Women's Ultra Mega Recall: Undeclared Milk Allergen
GNC recalls Women's Ultra Mega dietary supplements due to undeclared milk. Check your bottle for lot number 3044FQ2024.
Stop using this now
Undeclared Allergen: Milk.
Contact the company
What happened, in plain English
Nutra Manufacturing is recalling GNC Women's Ultra Mega dietary supplements because they contain undeclared milk. This poses a risk to individuals with milk allergies or sensitivities who may not be aware of the ingredient. The affected product was distributed in Pennsylvania. Read more at govinfonow.com/recall/22894-gnc-women-s-ultra-mega-recall-undeclared-milk-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/22894-gnc-women-s-ultra-mega-recall-undeclared-milk-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-0626-2017
Cite this page
“GNC Women's Ultra Mega Recall: Undeclared Milk Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/22894-gnc-women-s-ultra-mega-recall-undeclared-milk-allergen. Based on FDA recall #F-0626-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0626-2017%22&limit=1).
Why it’s dangerous
The supplement contains undeclared milk, which can trigger allergic reactions in sensitive individuals. People relying on the ingredient list may unknowingly consume an allergen they need to avoid.
Who’s affected
Consumers who purchased GNC Women's Ultra Mega dietary supplements, particularly those with milk allergies or dairy sensitivities. The recall specifically affects bottles distributed in Pennsylvania.
How to tell if you have this one
Look for GNC Women's Ultra Mega dietary supplements in 180-caplet bottles. Check the label for GNC number 202422 and Nutra Manufacturing Lot Number 3044FQ2024.
- Brand
GNC- Category
Food
What to do — step by step
Stop consuming the product
Do not eat or take the recalled supplements if you have them in your possession.
Check your bottle details
Verify that your bottle matches GNC number 202422 and Lot Number 3044FQ2024.
Where it went and when
Where it was distributed
Distributed in Pennsylvania.
FDA distribution: “PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Pennsylvania.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
How many bottles are affected by this recall?
Approximately 12,534 bottles containing 180 caplets each are included in the recall.
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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-0626-2017 (November 10, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0626-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.