Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, in
Summary
The FDA issued a Class II for Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, by TKS Co-pack Manufacturing, LLC. Reason: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination..
Details
Source
Food Recall
External ID
H-0521-2026
Action Date
2026-02-18
Status
Completed
Category
food
Product Description
Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Sipping unit: two 15 count decorated boxes in a corrugated Aonic Master Shipper. Firm Name and Address on Label: Aonic Inc. 2261 MarketStreet #5416 San Francisco, CA 94114 USA.
Lot/Code Info: Lot 5349A BB 12/27; Lot 5363A BB 12/27
Quantity Affected: 780 individual bottles
Reason for Recall
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Distribution
Distributed to customer in Utah.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-15
Company
Lindon, UT
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 70 food recalls issued in the same week, part of 204 food-related FDA actions this month.
TKS Co-pack Manufacturing, LLC has 2 FDA actions in our database, including 2 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 (TKS Co-pack Manufacturing, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does TKS Co-pack Manufacturing, LLC have FDA actions?
TKS Co-pack Manufacturing, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0521-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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