TKS Co-pack Manufacturing Recalls Aonic Complete Hers Supplement Shots Over Bacterial Contamination Concerns
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TKS Co-pack Manufacturing, LLC is recalling 3,630 bottles of Aonic Complete Hers dietary supplement shots in Utah due to potential contamination with E.coli and other bacteria.
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, Food.
What Happened
TKS Co-pack Manufacturing, LLC, based in Lindon, Utah, has initiated a voluntary recall of its Aonic Complete Hers dietary supplement drink shots. The recall was prompted by the potential presence of bacterial contaminants, including coliforms, E.coli, and Pseudomonas aeruginosa. The FDA has classified this as a Class II recall, which was initiated by the firm on January 15, 2026.
Which Products Are Affected
The recall involves Aonic Complete Hers, a single-serving liquid dietary supplement drink shot. The following details identify the affected units:
- Product Name: Aonic Complete Hers
- Packaging: 34 ml (1.1 Fl oz) plastic bottle, induction sealed with a plastic lid. Shipping units consist of two 15-count decorated boxes in a corrugated Aonic Master Shipper.
- Lot Numbers: 5349A (Best By 12/27) and 5363A (Best By 12/27).
- Quantity: 3,630 individual bottles.
- Geographic Scope: Distributed to a customer in Utah.
- Label Information: Aonic Inc., 2261 Market Street #5416, San Francisco, CA 94114.
What You Should Do
Consumers who have purchased the affected lots of Aonic Complete Hers should immediately stop using the product. The recalling firm has notified customers through various channels, including email, fax, letter, and telephone. For further information regarding returns or disposal instructions, consumers may contact TKS Co-pack Manufacturing, LLC at their facility located at 2642 W 400 N Ste 700, Lindon, UT 84042.
Why This Matters
The potential presence of E.coli and Pseudomonas aeruginosa in a dietary supplement poses a significant health risk to consumers, as these pathogens can cause serious gastrointestinal illness and other infections.
Source
Information provided by the FDA under recall number H-0520-2026.
Original source: FDA Official Notice ↗
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