FDA Food recall ·
Aonic Complete Hers recall
- Recall number
- H-0520-2026
- Date
- (initiated January 15, 2026)
- Company / brand
- TKS Co-pack Manufacturing, LLC
2642 W 400 N Ste 700, Lindon, UT, United States - Category
- Food › Class II
- Classification
- Class II
- Status
- Completed
- Units affected
- 3630 individual bottles
- Hazard tags
- E. coli Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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.
Why was it recalled?
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot 5349A BB 12/27; Lot 5363A BB 12/27
Distribution
Distributed to customer in Utah.
States: Utah
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (food), recall H-0520-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.