Aonic Complete His — Class II food recall H-0521-2026
Completed recall by TKS Co-pack Manufacturing, LLC, reported 2026-02-18, distributed in UT. Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
| Recall number | H-0521-2026 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | TKS Co-pack Manufacturing, LLC, Lindon, UT, United States |
| Recall initiated | 2026-01-15 |
| Classified | 2026-02-20 |
| Reported by FDA | 2026-02-18 |
| Distributed | UT |
| Quantity | 780 individual |
| Reason classes | microbial contamination |
| Pathogens | e coli, pseudomonas |
| Lot numbers | 12/27, 5349ABB, 5363ABB |
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 for recall
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/H-0521-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.