Food recall

Garden Of Life Llc recall: Garden of Life, FYI ULTRA, ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement

Garden Of Life Llc, of West Palm Beach, FL, recalled Garden of Life, FYI ULTRA, ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement and 2 other products. The FDA's reason: “Undeclared Soy.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on October 19, 2023, and the FDA first listed it in its Enforcement Report of December 13, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Allergen not on the label

Status

Terminated

Closed February 14, 2024

The recall

Company
Garden Of Life Llc (West Palm Beach, FL)
Reason, in FDA's words
“Undeclared Soy.”
Where it was sold
Domestic and foreign distribution.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
93289

The 3 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0482-2024 Class II

    Garden of Life, FYI ULTRA, ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement, 120 Ultra Zorbe VEGETARIAN CAPSULES

    Codes: Lot Numbers: 50312871, 50293093, 50278965, 5028258 Exp. Dates: 10/2023-6/2024

    Quantity: 37, 424 bottles

  • F-0483-2024 Class II

    Garden of Life, RM-10, Organically Grown Mushrooms, 60 Vegetarian Caplets, Whole Food Dietary Supplement

    Codes: Lot Numbers: 50298707, 50315317, 50298646, 50283628 Exp. Dates: 1/2024-8/2024

    Quantity: 15,119 bottles

  • F-0484-2024 Class II

    Garden of Life, RM-10 ULTRA, Ultimate Immune System Support60 Vegetarian Caplets, Whole Food Dietary Supplement, 90 Ultra Zorbe Vegetarian Capsules

    Codes: Lot Numbers: 50304364, 50298662 Exp. Dates: 2/2024-9/2024

    Quantity: 8,940 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of December 13, 2023.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.