TKS Co-pack Manufacturing Recalls Aonic Complete His Supplement Due to Potential Bacterial Contamination
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TKS Co-pack Manufacturing, LLC has voluntarily recalled Aonic Complete His dietary supplement shots in Utah due to possible E.coli and Pseudomonas aeruginosa contamination.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 6, 2026 and geographically references Utah. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, dietary-supplement.
What Happened
TKS Co-pack Manufacturing, LLC has initiated a voluntary recall of its Aonic Complete His dietary supplement drink shots. The recall was issued due to the potential presence of coliforms, E.coli, and/or Pseudomonas aeruginosa contamination, which was identified during testing.
Which Products Are Affected
The recall involves the following specific product lots:
- Product Name: Aonic Complete His
- Description: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in a plastic bottle, induction sealed with a plastic lid.
- Lot Numbers: 5349A (Best By 12/27) and 5363A (Best By 12/27).
- Quantity: 780 individual bottles.
- Distribution: These products were distributed to a customer in Utah.
- Label Details: The label lists Aonic Inc., 2261 Market Street #5416, San Francisco, CA 94114.
What You Should Do
Consumers who have purchased Aonic Complete His from the affected lots should stop using the product immediately. For information regarding refunds or product disposal, consumers should contact TKS Co-pack Manufacturing, LLC at their Lindon, Utah facility. The recall is being conducted with the knowledge of the FDA under recall number H-0521-2026.
Why This Matters
Contamination with pathogens such as E.coli and Pseudomonas aeruginosa poses a serious health risk to consumers. Ingestion of these bacteria can lead to severe gastrointestinal illness and other potentially life-threatening infections.
Source
Information provided by the FDA (Recall Number: H-0521-2026).
Original source: FDA Official Notice ↗
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