Quick Facts at a Glance
- Recall Date
- January 15, 2026
- Hazard Level
- HIGH
- Brand
- TKS Co-pack Manufacturing
- Category
- Food & Beverages
- Sold At
- Unknown
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- TKS Co-pack Manufacturing
- Product type
- Liquid Dietary Supplement
- Model numbers
- Lot 5349A BB 12/27, Lot 5363A BB 12/27
- Sold at
- Unknown
- Where affected
- UT
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 15, 2026
Reported by FDA FOOD
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
What You Should Do
Consumers who have purchased this product should not consume it. Contact TKS Co-pack Manufacturing, LLC for refund or replacement information. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
About This Product
Aonic Complete is a liquid dietary supplement shot designed to provide nutritional support in a convenient format. Consumers typically purchase these supplements for health benefits such as energy or immune support.
Why This Is Dangerous
The product may contain harmful bacteria that can cause serious health issues if ingested. Contamination can occur during manufacturing or packaging processes.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers should stop using the product immediately to avoid potential health risks. The recall may cause inconvenience for those relying on this supplement for dietary support.
Practical Guidance
How to identify if yours is affected
- Check the lot number on your bottle.
- Verify if the lot number matches Lot 5349A BB 12/27 or Lot 5363A BB 12/27.
- If your lot number matches, stop using the product immediately.
Where to find product info
Lot numbers are typically located on the bottom or side of the bottle.
What timeline to expect
Expect a refund or replacement process to take 4-6 weeks.
If the manufacturer is unresponsive
- Document your communication attempts with the company.
- Reach out to the FDA for further assistance if needed.
- Consider filing a complaint if you do not receive a timely response.
How to prevent similar issues
- Research brands before purchasing dietary supplements.
- Look for third-party testing or certifications.
- Review product recalls regularly.
Documentation advice
Keep receipts, correspondence with the manufacturer, and any photos of the product as records.
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Product Details
The recalled product is Aonic Complete, a single-serving liquid dietary supplement drink shot packaged in 34 ml plastic bottles. The affected lots include Lot 5349A BB 12/27 and Lot 5363A BB 12/27. The product was distributed to customers in Utah.
Key Facts
- Recall date: January 15, 2026
- Report date: February 18, 2026
- Distribution limited to Utah
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Safety Guide
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