Skip to content
Back to recalls
Food FDA Class II Completed Pathogen contamination

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 A

TKS Co-pack Manufacturing, LLC Published Feb 18, 2026

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 65/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact TKS Co-pack Manufacturing, LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall

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

Hazards

Escherichia coli O157:H7 · primaryColiforms Pseudomonas aeruginosa

Affected products (1)

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.

3630 individual bottles

Lot codes: 5349A, 5363A
Code info: Lot 5349A BB 12/27; Lot 5363A BB 12/27

Affected areas

Utah

Timeline

  1. Initiated
    Jan 15, 2026
  2. Published
    Feb 18, 2026
Recall number
H-0520-2026
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.