FDA recall H-0520-2026 · Feb 18, 2026
TKS Co-pack Manufacturing, LLC: Aonic Complete Hers recall
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.
Reason for recall
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Completed
- Codes, lots and dates
- Lot 5349A BB 12/27; Lot 5363A BB 12/27
- Quantity
- 3630 individual bottles
- Distribution
- Distributed to customer in Utah.
- Recalling firm
- TKS Co-pack Manufacturing, LLC, Lindon, UT
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-01-15
Source: openFDA enforcement record H-0520-2026 · search recall number H-0520-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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