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Class II: temporary or reversible health riskCompleted

TKS Co-pack Manufacturing Aonic Complete Hers Recall

Aonic Complete Hers

TKS Co-pack Manufacturing, LLC · Lindon, UT

Risk level
Class II
Reported by FDA
Feb 18, 2026
Recall ID
H-0520-2026
Check your lot numberHow we source this data

Summary

TKS Co-pack Manufacturing recalled Aonic Complete Hers starting Jan 15, 2026. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0520-2026 on Feb 18, 2026. Reason: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. Status: Completed.

Why it was recalled

Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.

Product description

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.

Lot numbers, UPCs & expiration codes

Lot 5349A BB 12/27; Lot 5363A BB 12/27

Where it was sold

Distributed to customer in Utah.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0520-2026
Classification
Class II
Status
Completed
Recall initiated
Jan 15, 2026
FDA report date
Feb 18, 2026
Quantity
3630 individual bottles
Recall type
Voluntary: Firm initiated
Recalling firm
TKS Co-pack Manufacturing, LLC

Original FDA data

Every field from FDA enforcement report H-0520-2026, exactly as published.

Show all FDA fields
City
Lindon
State
UT
Status
Completed
Country
United States
Event ID
98325
Address
2642 W 400 N Ste 700
Code information
Lot 5349A BB 12/27; Lot 5363A BB 12/27
Postal code
84042-1142
Report date
Feb 18, 2026
Product type
Food
Recall number
H-0520-2026
Classification
Class II
Recalling firm
TKS Co-pack Manufacturing, LLC
Product quantity
3630 individual bottles
Reason for recall
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
Distribution pattern
Distributed to customer in Utah.
Recall initiation date
Jan 15, 2026
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Feb 20, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0520-2026, published Feb 18, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

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