Class IICompletedVoluntary: Firm initiated
TKS Co-pack Manufacturing, LLC: food recall H-0520-2026
TKS Co-pack Manufacturing, LLC of Lindon, UT recalled Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle,… Reason: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. The FDA listed it as Class II in its Enforcement Report dated Feb 18, 2026; distribution: Utah.
Record status as published: Completed. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Aonic Complete Hers. 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. Shipping 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.
- Product quantity
- 3630 individual bottles
- Reason for recall
- Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
- Codes, lots and dates on the package
- Lot 5349A BB 12/27; Lot 5363A BB 12/27
- Distribution pattern
- Distributed to customer in Utah.
- Recalling firm
- TKS Co-pack Manufacturing, LLC, Lindon, UT
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jan 15, 2026 |
| Classified by the FDA | Feb 20, 2026 |
| Published in the Enforcement Report | Feb 18, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 98325).
- 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…
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0520-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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