FDA recall, , Moderate risk
Aonic Complete Hers and His
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Summary by Recall Canary from the FDA notice
What happened
TKS Co-pack Manufacturing, LLC of Lindon, Utah recalled Aonic Complete His and Aonic Complete Hers liquid dietary supplement drink due to possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. The products, each a 34 ml (1.1 Fl oz) single serving in a plastic bottle, were distributed to a customer in Utah. The recall began January 15, 2026, and was added to the FDA's Enforcement Report on February 12, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is your bottle affected?
2 products
Affected if its lot code is listed.
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
- Lot code
- 5349A
- 5363A
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
- Lot code
- 5349A
- 5363A
Recall details
- Company began the recall
- Sold in
Distributed to customer in Utah.
- Company
- TKS Co-pack Manufacturing, LLCLindon, Utah
- Hazard
- E. coli
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98325
- Recall numbers
- H-0520-2026 to H-0521-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Classified by FDA
Listed on Recall Canary
Summary updated
