Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 9, 2025 (13 months ago)

Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint recall

Recalled by Eden¿¿¿s Elixirs, LLC · Louisville, CO, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared Yellow #5

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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.

Quantity: 141,000 tablets

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Code: F250160, Packing Code: 250152

Where it was sold

Texas

FDA's distribution note: Distributed in Texas.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Eden¿¿¿s Elixirs, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 9, 2025
In FDA report of
Oct 15, 2025
Terminated
May 15, 2026
FDA recall number
H-0131-2026 · event 97593
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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