TKS Co-pack Manufacturing, LLC recalls Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot
TKS Co-pack Manufacturing, LLC started this recall on January 15, 2026. The FDA classified it as Class II, a middle category: eating the product may cause temporary or medically reversible health problems, and serious harm is unlikely. The reason given is e. coli. It was distributed in 1 state. This recall is no longer considered active, but recalled products can stay in pantries and freezers for months.
- Status
- Closed / older
- Recall started
- January 15, 2026
- Company
- TKS Co-pack Manufacturing, LLC
- Classification
- Class II (temporary or reversible health risk)
- Where sold
- Utah
- Quantity
- 3630 individual bottles; 780 individual bottles
Reason for recall (official wording)
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Recalled products (official wording)
- 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.
- 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.
Distribution
Distributed to customer in Utah.
What to do
Compare the brand, size, lot code and dates on your package with the details above. If they match, do not eat it. Throw it away or return it to the store. Contact a healthcare provider if you feel unwell. Step-by-step guide.
Source: FDA Enforcement Report (openFDA), event 98325.