Lifted Made-Lemon, Chewable tablet. 20mg 7OH/550mg Tablet-no shelf-life. Dosage: 2 doses per…
Recalling firm: Eden¿¿¿s Elixirs, LLC
Undeclared Yellow #5
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 15, 2026.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
Lot Code: F250129, Packing Code: 250023 Lot Code: F250150, Packing Code: 250147 Lot Code: F250166, Packing Code: 250156
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
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.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | F250129 | Lot Code: F250129, Packing Code: 250023 Lot Code: F250150, Packing Code: 250147 Lot Code: F250166, Packing Code: 250156 |
| lot | F250150 | Lot Code: F250129, Packing Code: 250023 Lot Code: F250150, Packing Code: 250147 Lot Code: F250166, Packing Code: 250156 |
| lot | F250166 | 50129, Packing Code: 250023 Lot Code: F250150, Packing Code: 250147 Lot Code: F250166, Packing Code: 250156 |
Original FDA recall reason
Undeclared Yellow #5
Recall details
- Recall number
- H-0129-2026
- Event ID
- 97593
- FDA status
- Terminated
- Initiated
- Sep 9, 2025
- Reported
- Oct 15, 2025
- Classified
- Oct 23, 2025
- Terminated
- May 15, 2026
- Quantity
- 284,354 tablets
- Location
- Louisville, CO, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Distributed in Texas.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.