Aonic Complete His recalled over E. coli risk

Recall date

January 15, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

TKS Co-pack Manufacturing, LLC recalls Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, i…

Recall number

H-0521-2026

FDA classification

Class II

Brand / firm

TKS Co-pack Manufacturing, LLC

Sold / distributed

Distributed to customer in Utah.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

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.