Market America Recalls Bliss Anti-Stress Formula Due to Undeclared Yohimbe
Market America recalls 60-tablet bottles of Bliss Anti-Stress Formula due to undeclared Yohimbe, which can cause adverse reactions like dizziness and upset stomach.
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Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.
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What happened, in plain English
Market America Inc is recalling its Bliss Anti-Stress Formula dietary supplement because it may contain undeclared Yohimbe. Consumers have reported adverse reactions such as upset stomach, jitteriness, sweating, lightheadedness, or dizziness after taking the product. The recall affects specific bottles distributed across the United States and several international locations. Read more at govinfonow.com/recall/20317-market-america-recalls-bliss-anti-stress-formula-due-to-undeclared.
Source Summary by GovInfoNow · govinfonow.com/recall/20317-market-america-recalls-bliss-anti-stress-formula-due-to-undeclared · Updated October 11, 2026 · FDA enforcement record: FDA #F-0681-2020
Cite this page
“Market America Recalls Bliss Anti-Stress Formula Due to Undeclared Yohimbe.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20317-market-america-recalls-bliss-anti-stress-formula-due-to-undeclared. Based on FDA recall #F-0681-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0681-2020%22&limit=1).
Why it’s dangerous
The product contains undeclared Yohimbe, a substance not listed on the label. This can lead to unexpected adverse reactions including upset stomach, jitteriness, sweating, lightheadedness, or dizziness in users.
Who’s affected
Consumers who purchased the Bliss Anti-Stress Formula dietary supplement between the manufacturing date and July 2019, particularly those in the listed U.S. states, Australia, Canada, and Hong Kong. Individuals sensitive to stimulants or those experiencing symptoms like dizziness or jitteriness are at risk.
How to tell if you have this one
Check for bottles labeled 'bliss anti-stress formula Dietary Supplement' containing 60 Tablets. Look for UPC 8 48570 00470 3, Lot # 51130, Expiration Date 07/2019, Manufacturer's Code PK-MA13173, and Manufacturer's Item #Z02320. The product was distributed in many U.S. states as well as Australia, Canada, and Hong Kong.
- Brand
Market America- Product
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc- Category
Food
Where it went and when
Where it was distributed
Distributed in 46 states, and outside the U.S.
FDA distribution: “Product was shipped to the following states: AK, AL, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI & WV.…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Alaska, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 2.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
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-0681-2020 (October 19, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0681-2020 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.