Food recall

Edens Elixirs, LLC recall: Lifted Made-Lemon, Chewable tablet

Edens Elixirs, LLC, of Louisville, CO, recalled Lifted Made-Lemon, Chewable tablet and 2 other products. The FDA's reason: “Undeclared Yellow #5.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on September 9, 2025, and the FDA first listed it in its Enforcement Report of October 15, 2025. 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

Other ingredient not on the label (sulfites, dyes...)

Status

Terminated

Closed May 15, 2026

The recall

Company
Edens Elixirs, LLC (Louisville, CO)
Reason, in FDA's words
“Undeclared Yellow #5”
Where it was sold
Distributed in Texas.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97593

The 3 products recalled

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

  • H-0129-2026 Class II

    Lifted Made-Lemon, Chewable tablet. 20mg 7OH/550mg Tablet-no shelf-life. Dosage: 2 doses per tablet. Route of administration: oral. Shipping or unit package 10,000 or less per bulk bag. Bulk package and is not sold directly to consumer.

    Codes: Lot Code: F250129, Packing Code: 250023 Lot Code: F250150, Packing Code: 250147 Lot Code: F250166, Packing Code: 250156

    Quantity: 284,354 tablets

  • H-0130-2026 Class II

    Eskay Brands Mint flavored tablets. 40mg 7OH/550mg Tablet- Eskay Brands-Mint, Chewable tablet, no shelf-life. Dosage: 2 doses per tablet. 10,000 or less per bulk bag. Bulk package and is not sold directly to consumer.

    Codes: Lot Code: F250136, Packing Code: 250030

    Quantity: 10,000 tablets

  • H-0131-2026 Class II

    Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint, Chewable tablet, no shelf-life. Dosage: 2 doses per tablet. Shipping or unit package: 10,000 or less per bulk bag. Bulk package and is not sold directly to consumer.

    Codes: Lot Code: F250160, Packing Code: 250152

    Quantity: 141,000 tablets

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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 October 15, 2025.

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.