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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
Food & Beverages/Dietary Supplements

Garden of Life Dietary Supplements Recalled for Undeclared Soy

Agency Publication Date: December 1, 2023
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Summary

Garden of Life LLC has recalled 61,483 bottles of FYI ULTRA, RM-10, and RM-10 ULTRA dietary supplements because they contain soy that is not listed on the label. The recall includes Joint & Cartilage formulas and Immune System Support supplements sold in various bottle sizes. No injuries or illnesses have been reported to date regarding this recall. Consumers with an allergy or sensitivity to soy should not consume these products, as it may cause a serious allergic reaction.

Risk

People with an allergy or severe sensitivity to soy are at risk of a serious or life-threatening allergic reaction if they consume these supplements. The presence of undeclared soy is the result of a labeling error.

What You Should Do

  1. This recall affects Garden of Life brand FYI ULTRA (120 capsules), RM-10 (60 caplets), and RM-10 ULTRA (60 caplets or 90 capsules) dietary supplements.
  2. Check your supplement bottles for the following lot numbers: FYI ULTRA (50312871, 50293093, 50278965, 5028258); RM-10 (50298707, 50315317, 50298646, 50283628); and RM-10 ULTRA (50304364, 50298662).
  3. Return the product to the place of purchase for a refund, throw it away, or contact Garden of Life LLC for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional information about this recall.

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: Garden of Life FYI ULTRA ULTIMATE Joint & Cartilage Formula (120 capsules)
Variants: 120 Ultra Zorbe VEGETARIAN CAPSULES
Lot Numbers:
50312871
50293093
50278965
5028258
Date Ranges: Expiration dates: 10/2023 - 6/2024

Recall #: F-0482-2024; Quantity: 37,424 bottles

Product: Garden of Life RM-10 Organically Grown Mushrooms (60 caplets)
Variants: 60 Vegetarian Caplets
Lot Numbers:
50298707
50315317
50298646
50283628
Date Ranges: Expiration dates: 1/2024 - 8/2024

Recall #: F-0483-2024; Quantity: 15,119 bottles

Product: Garden of Life RM-10 ULTRA Ultimate Immune System Support (60 caplets or 90 capsules)
Variants: 60 Vegetarian Caplets, 90 Ultra Zorbe Vegetarian Capsules
Lot Numbers:
50304364
50298662
Date Ranges: Expiration dates: 2/2024 - 9/2024

Recall #: F-0484-2024; Quantity: 8,940 bottles

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93289
Status: Resolved
Manufacturer: Garden Of Life Llc
Sold By: Domestic and foreign distribution
Manufactured In: United States
Units Affected: 3 products (37, 424 bottles; 15,119 bottles; 8,940 bottles)
Distributed To: Nationwide

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.