Evexias Health Solutions Amino Ultra, 90-capsules, dietary supplement in white plastic bottles with blue/green/white lab
Summary
The FDA issued a Class II for Evexias Health Solutions Amino Ultra, 90-capsules, dietary supplement in white p by EVEXIAS HEALTH SOLUTION. Reason: The product is mislabeled and fails to declare fish oil..
Details
Source
Food Recall
External ID
H-0170-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
Evexias Health Solutions Amino Ultra, 90-capsules, dietary supplement in white plastic bottles with blue/green/white labeling
Lot/Code Info: " Lot Number: 594886001 MFG 1125, printed on side label. " Affected units only: Bottles with 496 inkjet-printed on the bottom
Quantity Affected: 30 bottles
Reason for Recall
The product is mislabeled and fails to declare fish oil.
Distribution
FL, NM, PA, NY, TN, SD, ND, KY, WA
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-24
Company
Southlake, TX
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 82 food recalls issued in the same week, part of 117 food-related FDA actions this month.
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 (EVEXIAS HEALTH SOLUTION) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does EVEXIAS HEALTH SOLUTION have FDA actions?
This is the only FDA action we have on record for EVEXIAS HEALTH SOLUTION in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0170-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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