Customer reports of label error. Front panel states strength of 1000 mg although supplement fact is correct in stating 1000 mcg.
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📍Recalling firmNational Vitamin Company Inc1145 W Gila Bend Hwy · Casa Grande, AZ 85122-4308
✎ GovInfoNow plain-language explainer
National Vitamin Company Inc is recalling Nature's Blend Folic Acid 1000 mcg dietary supplements because the front panel incorrectly states the strength as 1000 mg, while the supplement facts list the correct amount of 1000 mcg. This label error affects approximately 3,370 bottles distributed across several U.S. states. The record does not specify a remedy or indicate that the product poses an immediate physical danger. Read more at govinfonow.com/recall/15824-nature-s-blend-folic-acid-recall-label-error-on-1000.
“Nature's Blend Folic Acid Recall: Label Error on 1000 mcg Bottles.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/15824-nature-s-blend-folic-acid-recall-label-error-on-1000. Based on FDA recall #F-0872-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0872-2020%22&limit=1).
The FDA announced on Feb. 28, 2020, that National Vitamin Company Inc is recalling Nature's Blend Folic Acid dietary supplements due to a label error stating 1000 mg instead of the correct 1000 mcg strength. Consumers should stop using the product and contact the company for a refund.
Sold in AZ, FL, GA, IL, MA, MI, MT, ND, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA
The hazard
The front panel of the supplement bottle incorrectly states the strength as 1000 mg, although the supplement facts panel correctly lists 1000 mcg. The FDA cited customer reports of this labeling discrepancy as the basis for the recall.
Context
GovInfoNow's records show other recent recalls of similar products include Shaman Botanicals Recalls White Vein Chewable Tablets Due to Dosage Error (2026-02-13), Prospector Popcorn Recall: Nutrient Labeling Error (2026-07-15), and Winder Labs Recalls Grape Multivitamins Due to Subpotent Vitamin D (2025-10-27).
How to tell if you have this one
Check if you have a 1000-count bottle of Nature's Blend Folic Acid 1000 mcg Dietary Supplement with Product Number 1280 and UPC 0-79854-51280-9. Verify the lot numbers are 9JA08 or 9JA09 and the expiration date is 10/22.
FDA distribution: “AZ. FL, GA, IL, MA, MI, MT, ND, NJ, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Florida, Georgia, Illinois, Massachusetts, Michigan, Montana, New Jersey, New York, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
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-0872-2020 (February 28, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0872-2020 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.