Food recall

TKS Co-pack Manufacturing, LLC recall: Aonic Complete Hers

TKS Co-pack Manufacturing, LLC, of Lindon, UT, recalled Aonic Complete Hers and 1 other product. The FDA's reason: “Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on January 15, 2026, and the FDA first listed it in its Enforcement Report of February 18, 2026. The company has finished the recall; the FDA hasn't closed it yet.

How serious

Class II

It could cause temporary or minor harm

Why

E. coli

Status

Completed

The recall

Company
TKS Co-pack Manufacturing, LLC (Lindon, UT)
Reason, in FDA's words
“Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.”
Where it was sold
Distributed to customer in Utah.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
98325

The 2 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0520-2026 Class II

    Aonic Complete Hers. 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. Shipping 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.

    Codes: Lot 5349A BB 12/27; Lot 5363A BB 12/27

    Quantity: 3630 individual bottles

  • H-0521-2026 Class II

    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.

    Codes: Lot 5349A BB 12/27; Lot 5363A BB 12/27

    Quantity: 780 individual bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of February 18, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.