CLASS II Food recall · Reported 18 Feb 2026 · FDA Enforcement Report
Aonic Complete Hers recalled by TKS Co-pack Manufacturing
TKS Co-pack Manufacturing is recalling Aonic Complete Hers, distributed in Utah. The recall was initiated on 15 Jan 2026 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0520-2026
- FDA event ID
- 98325
- Recalling firm
- TKS Co-pack Manufacturing, Lindon, UT
- Brand
- Aonic Complete
- Classification
- Class II
- Status
- Completed
- Recall initiated
- 15 Jan 2026
- FDA classified
- 20 Feb 2026
- Reported
- 18 Feb 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- E. coli
- Product category
- Dietary Supplements
Timeline
| 15 Jan 2026 | Recall initiated by company | |
| 18 Feb 2026 | Published in enforcement report | +34 days |
| 20 Feb 2026 | Classified by FDA | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.
Product as listed by the FDA
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.
Where it was distributed
Distributed to customer in Utah.
Questions about this recall
Is Aonic Complete Hers recalled?
Yes. TKS Co-pack Manufacturing recalled Aonic Complete Hers on 15 Jan 2026. The recall is Class II and its status is Completed. Recall number H-0520-2026.
Why was it recalled?
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Which lots are affected?
Lot 5349A BB 12/27; Lot 5363A BB 12/27
Where was it sold?
Distributed to customer in Utah.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from TKS Co-pack Manufacturing
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Aonic Complete His recalled by TKS Co-pack ManufacturingAonic Complete | TKS Co-pack Manufacturing | E. coli | UT |
Other Dietary Supplements recalls
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|---|---|---|---|---|---|
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |