Aonic Complete Hers recall
Recalled by TKS Co-pack Manufacturing, LLC
The product, as the FDA describes it: 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.
Why it was recalled
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
What to do if you have it
Nothing about aonic complete hers will look or smell wrong, because the organisms behind this kind of recall leave no trace you can see or taste. Do not cook it to make it safe and do not sample it. Throw it out or return it, then wash anything it touched, including the shelf it sat on and the container beside it.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
Lot 5349A BB 12/27; Lot 5363A BB 12/27
The details on record
| Recalling company | TKS Co-pack Manufacturing, LLC |
|---|---|
| Company location | Lindon, UT |
| Where it was distributed | Distributed to customer in Utah. |
| How much was recalled | 3630 individual bottles |
| Recall started | January 15, 2026 |
| Published by the FDA | February 18, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| FDA recall number | H-0520-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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