Aonic Complete His. Dosage: Single serving liquid dietary supplemen…
Recalled by TKS Co-pack Manufacturing, LLC
Food recall
TKS Co-pack Manufacturing, LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
TKS Co-pack Manufacturing, LLC has recalled Aonic Complete His. Dosage: Single serving liquid dietary supplemen…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 18, 2026 and was initiated on January 15, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Aonic Complete His. Dosage: Single serving liquid dietary supplemen…, with approximately 780 individual bottles affected. The company behind the recall is TKS Co-pack Manufacturing, LLC, based in Lindon, UT. The FDA describes the product as: “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…”
Why was Aonic Complete His. Dosage: Single serving liquid dietary supplemen… recalled?
According to the FDA, the stated reason for the recall is: “Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.” In plain terms, this recall relates to E. coli.
Escherichia coli (E. coli) is a large group of bacteria. While most types are harmless, certain strains such as O157:H7 can produce toxins that cause illness. Public health agencies note that symptoms can include severe stomach cramps, diarrhea, and vomiting, with young children and older adults facing a greater risk of complications.
What should you do?
If you think you may have bought Aonic Complete His. Dosage: Single serving liquid dietary supplemen…, compare it against the product description and identifying codes (Lot 5349A BB 12/27; Lot 5363A BB 12/27) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact TKS Co-pack Manufacturing, LLC or your local health authority.
About this recall
This recall was distributed in UT. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Completed
- Date reported
- February 18, 2026
- Recall started
- January 15, 2026
- Distributed in
- UT
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Aonic Complete His. Dosage: Single serving liquid dietary supplemen… recalled?+
According to the FDA: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Aonic Complete His. Dosage: Single serving liquid dietary supplemen…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0521-2026. Information last synced from the FDA on July 5, 2026.