Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint, Chewable tablet, no shelf-life. Dosage: 2 dos
Summary
The FDA issued a Class II for Lifted Made Mint flavored tablets 20mg 7OH/550mg Tablet- Lifted Made-Mint, Chewa by Eden¿¿¿s Elixirs, LLC. Reason: Undeclared Yellow #5.
Details
Source
Food Recall
External ID
H-0131-2026
Action Date
2025-10-15
Status
Terminated
Category
food
Product Description
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.
Lot/Code Info: Lot Code: F250160, Packing Code: 250152
Quantity Affected: 141,000 tablets
Reason for Recall
Undeclared Yellow #5
Distribution
Distributed in Texas.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-09
Company
Louisville, CO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Eden¿¿¿s Elixirs, LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Eden¿¿¿s Elixirs, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Eden¿¿¿s Elixirs, LLC have FDA actions?
Eden¿¿¿s Elixirs, LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0131-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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