Food recall: Lifted Made-Lemon, Chewable tablet. 20mg 7OH/550mg Tablet-no shelf-life. Dosage: 2 doses per tablet. Route of administra
Eden¿¿¿s Elixirs, LLC (Louisville, CO) initiated this food recall on 9 Sep 2025; FDA lists 3 product records under event 97593, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 54% of the 569 food enforcement events initiated in 2025 carry the same class.
Status: Terminated, terminated 15 May 2026. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Eden¿¿¿s Elixirs, LLC.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Eden¿¿¿s Elixirs, LLC, Louisville, CO.
Reason for recall
"Undeclared Yellow #5"
Distribution
"Distributed in Texas."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| H-0129-2026 | 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. | 284,354 tablets | Class II | Terminated | 15 Oct 2025 |
| H-0130-2026 | 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. | 10,000 tablets | Class II | Terminated | 15 Oct 2025 |
| H-0131-2026 | 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. | 141,000 tablets | Class II | Terminated | 15 Oct 2025 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Undeclared Yellow #5"
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "Distributed in Texas."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 15 May 2026. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.