Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl…
Recalling firm: TKS Co-pack Manufacturing, LLC
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Historical recall record. This is not a new recall announcement. “Completed” describes the FDA recall process; it does not certify that an individual package is safe.
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FDA code information
Lot 5349A BB 12/27; Lot 5363A BB 12/27
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Full FDA record and distribution details
Original product description
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.
Original FDA recall reason
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Recall details
- Recall number
- H-0521-2026
- Event ID
- 98325
- FDA status
- Completed
- Initiated
- Jan 15, 2026
- Reported
- Feb 18, 2026
- Classified
- Feb 20, 2026
- Quantity
- 780 individual bottles
- Location
- Lindon, UT, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Distributed to customer in Utah.
Data updated September 16, 2026. View official FDA data ↗
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