Food Recall Check
Class II · Moderate risk Completed Initiated Jan 15, 2026 (9 months ago)

Aonic Complete His recall

Recalled by TKS Co-pack Manufacturing, LLC · Lindon, UT, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.

Pathogen: E. coli

Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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.

Quantity: 780 individual bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Utah

FDA's distribution note: Distributed to customer in Utah.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as completed: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
TKS Co-pack Manufacturing, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 15, 2026
In FDA report of
Feb 18, 2026
FDA recall number
H-0521-2026 · event 98325
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Completed E. coli

Aonic Complete Hers

Reason Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.

TKS Co-pack Manufacturing, LLC UT H-0520-2026

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