Garry N Sun Mahayograj Guggulu Dietary Supplement Recall: High Lead Levels Found
Garry N Sun USA Inc. recalls Mahayograj Guggulu dietary supplements due to high lead levels detected in consumer samples. This recall affects 120 vegetarian capsules and 1/2 lb. bags of powder sold in Reno, NV.
“Garry N Sun Mahayograj Guggulu Dietary Supplement Recall: High Lead Levels Found.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14505-garry-n-sun-mahayograj-guggulu-dietary-supplement-recall-high-lead. Based on FDA recall #F-0633-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0633-2021%22&limit=1).
The FDA announced on May 17, 2021, that Garry N Sun USA Inc. voluntarily recalled Mahayograj Guggulu dietary supplements due to high levels of lead. The Class I recall affects products distributed in multiple U.S. states and countries.
The Iowa Department of Agriculture and Land Stewardship collected a consumer sample and found lead levels of 12,200 mg/kg. The FDA classified this as a Class I recall, the most serious category.
Context
GovInfoNow's records show other recent recalls of similar products include U.S. Trading Company Dragonfly Thai Ginger Powder Recall (2026-05-15), Venzu Traders Cinnamon Powder Recall (2025-11-14), and Sonex Aluminum Pot Recall (2025-11-19).
How to tell if you have this one
Check for the product name 'Mahayograj Guggulu' with 120 vegetarian capsules or 1/2 lb. bags of powder. The product was distributed by Garry N Sun USA Inc. from 1030 Matley Lane, Unit A, Reno, NV 89502.
Brand
Garry N Sun
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the product name 'Mahayograj Guggulu' with 120 vegetarian capsules or 1/2 lb. bags of powder.
Where it went and when
Where it was distributed
Distributed in 11 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “North Carolina, Arkansas, Hawaii, Idaho, New Mexico, Texas, Florida, Arizona, Washington, Michigan, California, Canada, Germany.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Arkansas, California, Florida, Hawaii, Idaho, Michigan, New Mexico, North Carolina, Texas, Washington.
Recall timeline
FDA terminated this recall 46 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
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-0633-2021 (May 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0633-2021 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.