Warning
TKS Co-pack Manufacturing Recalls Aonic Complete His
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #H-0521-2026Food
TKS Co-pack Manufacturing Recalls Aonic Complete His
TKS Co-pack Manufacturing, LLC · Class II — Moderate Risk
Product Description
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.
Reason for Recall
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Distributed to customer in Utah.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the food product may cause temporary health problems or poses a slight threat of a serious nature. TKS Co-pack Manufacturing, LLC initiated the recall on January 15, 2026 affecting 780 individual bottles. Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. The product was distributed in Distributed to customer in Utah. Consumers should check their purchases and discontinue use of any affected product. Contact TKS Co-pack Manufacturing, LLC for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Food Contamination.