Recall map → All recalls → H-0521-2026
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. TKS Co-pack Manufacturing, LLC · reported 2026-02-18
Completed The agency has not recorded this recall as closed out.
- Reason for recall
- Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
- Classification
- Class II
- Recall initiated
- 2026-01-15
- Reported by the agency
- 2026-02-18
- Closed out (terminated)
- not reported
- Recalling firm
- TKS Co-pack Manufacturing, LLC
Lindon, UT
United StatesThis is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
- Distribution (the agency's own words)
- Distributed to customer in Utah.
- States we parsed from that text
- UT
The agency named these states. Parse method explicit_state_list, confidence high.
- Food category
- Beverages Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
- Recall type
- Voluntary: Firm initiated
- Recall number
- H-0521-2026
View this record at the agency source →
This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.