BrainMD recalls 120-capsule Brain & Memory Power Boost supplement due to containing NeuroVite Plus vitamins instead of intended ingredients. Consumers should check UPC 857568003413 for affected units.
“BrainMD Brain & Memory Power Boost Capsules Recall: Wrong Product Inside.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14160-brainmd-brain-memory-power-boost-capsules-recall-wrong-product-inside. Based on FDA recall #F-0010-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0010-2022%22&limit=1).
The FDA announced on Sept. 9, 2021, that BrainMD voluntarily recalled its Brain MD - Brain & Memory Power Boost dietary supplement because bottles were filled with a different product. The agency issued recall number F-0010-2022 for the Class II violation.
The recall occurred because bottles of Brain and Memory Power Boost were filled with a multi vitamin-mineral product called NeuroVite Plus. The FDA classified this mislabeling as a Class II hazard.
Context
GovInfoNow's records show the brand has been involved in other recent recalls, including a March 12, 2026, recall of Yunker Energy & Health Herbal Supplement for unmet Vitamin E claims and a May 7, 2026, recall of Llorens Vitamin B-Complex Supplement due to black particulate matter. Other recent recalls of similar products include the Nutricia Liquid Hope Organic Whole Foods Meal Replacement recall on May 26, 2026, which cited a Vitamin A testing error.
How to tell if you have this one
Check for the UPC 857568003413 on the bottle. The product was distributed with lot number N21301001 and best by date 10/1/2022.
Brand
BrainMD
Product
Brain MD - Brain & Memory Power Boost Supports Healthy Brain and Memory Performance 120 capsules - Dietary Supplement
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the UPC 857568003413 on the bottle label to confirm if it's affected.
How this recall unfolded
Recall timeline
FDA terminated this recall 50 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0010-2022 (September 9, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0010-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.