CLASS II Food recall · Reported 15 Oct 2025 · FDA Enforcement Report
Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet recalled
Eden¿¿¿s Elixirs is recalling Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint, Chewable, distributed in Texas. The recall was initiated on 9 Sep 2025 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0131-2026
- FDA event ID
- 97593
- Recalling firm
- Eden¿¿¿s Elixirs, Louisville, CO
- Brand
- Lifted Made
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 9 Sep 2025
- FDA classified
- 23 Oct 2025
- Reported
- 15 Oct 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Allergens
- Product category
- Other
Timeline
| 9 Sep 2025 | Recall initiated by company | |
| 15 Oct 2025 | Published in enforcement report | +36 days |
| 23 Oct 2025 | Classified by FDA | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Yellow #5
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
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.
Where it was distributed
Distributed in Texas.
Questions about this recall
Is Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint, Chewable recalled?
Yes. Eden¿¿¿s Elixirs recalled Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint, Chewable on 9 Sep 2025. The recall is Class II and its status is Terminated. Recall number H-0131-2026.
Why was it recalled?
Undeclared Yellow #5
Which lots are affected?
Lot Code: F250160, Packing Code: 250152
Where was it sold?
Distributed in Texas.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Eden¿¿¿s Elixirs
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Lifted Made-Lemon, Chewable tablet recalled by Eden¿¿¿s ElixirsLifted Made-Lemon | Eden¿¿¿s Elixirs | Undeclared Allergens | TX |
| Food | CLASS II | Eskay Brands Mint flavored tablets recalled by Eden¿¿¿s ElixirsEskay Brands | Eden¿¿¿s Elixirs | Undeclared Allergens | TX |
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