TKS Co-pack Manufacturing Recalls Aonic Complete Hers Supplement Shots Over Bacterial Contamination Concerns

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.