Recalls / Class II
Class IIH-0521-2026
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.
- Type
- Food
- Affected lot / code info
- Lot 5349A BB 12/27; Lot 5363A BB 12/27
- Quantity
- 780 individual bottles
Why it was recalled
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Recalling firm
- Firm
- TKS Co-pack Manufacturing, LLC
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 2642 W 400 N Ste 700, N/A, Lindon, Utah 84042-1142
Distribution
- Distribution pattern
- Distributed to customer in Utah.
Timeline
- Recall initiated
- 2026-01-15
- FDA classified
- 2026-02-20
- Posted by FDA
- 2026-02-18
- Status
- Completed
Source: openFDA Food Enforcement endpoint. Recall record H-0521-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings.