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TKS Co-pack Manufacturing, LLC
FDA recall H-0521-2026 · Class II · reported 2026-02-18 · Completed
- Product
- 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
- Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
- Quantity
- 780 individual bottles
- Distribution
- Distributed to customer in Utah.
- Firm location
- UT, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Recall started
- 2026-01-15
- Code info
- Lot 5349A BB 12/27; Lot 5363A BB 12/27
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.