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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Medications & Supplements/Dietary Supplements

Market America Bliss Anti-Stress Formula Recalled for Undeclared Yohimbe

Agency Publication Date: February 10, 2020
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Summary

Market America Inc. is recalling 1,496 bottles of Bliss Anti-Stress Formula dietary supplement because they may contain undeclared Yohimbe 83. The company has received reports of adverse reactions including upset stomach, jitters, sweating, and dizziness. The affected products were sold in 60-count tablet bottles and distributed across most U.S. states and several international locations.

Risk

The supplement contains Yohimbe 83, which is not listed on the label; consuming this undeclared ingredient can cause physical symptoms such as a racing heart, sweating, dizziness, and stomach upset.

What You Should Do

  1. Check your supplement bottles for 'bliss anti-stress formula' with UPC 8 48570 00470 3 and Lot number 51130 or PK-MA13173.
  2. Verify the expiration date on the bottle is 07/2019 and the manufacturer's item number is Z02320.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact Market America Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: bliss anti-stress formula Dietary Supplement (60 Tablets)by Market America Inc
Variants: 60 Tablets
Item Code:
Z02320
PK-MA13173
UPC Codes:
848570004703
Lot Numbers:
51130 (Exp 07/2019)
PK-MA13173

Manufactured For and distributed by: Market America, Inc., 1302 Pleasant Ridge Road, Greensboro, NC 27409

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84537
Status: Resolved
Manufacturer: Market America Inc
Sold By: Market America Inc
Manufactured In: United States
Units Affected: 1,496/60 tablet bottles
Distributed To: Alaska, Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, U.S. Virgin Islands, Vermont, Washington, Wisconsin, West Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.