FDA recall H-0131-2026 · Oct 15, 2025
Eden¿¿¿s Elixirs, LLC: Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint recall
Product
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.
Reason for recall
Undeclared Yellow #5
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Terminated
- Codes, lots and dates
- Lot Code: F250160, Packing Code: 250152
- Quantity
- 141,000 tablets
- Distribution
- Distributed in Texas.
- Recalling firm
- Eden¿¿¿s Elixirs, LLC, Louisville, CO
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-09-09
Source: openFDA enforcement record H-0131-2026 · search recall number H-0131-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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