Home / TKS Co-pack Manufacturing, LLC / H-0520-2026
Class II
TKS Co-pack Manufacturing, LLC
Recall #H-0520-2026 · Initiated 2026-01-15
Plain-language summary
by FoodRecallsDB.infoWhat happened
The FDA is recalling Aonic Complete Hers dietary supplement drinks because they may contain harmful bacteria (coliforms, E. coli, and/or Pseudomonas aeruginosa). About 3,630 bottles were distributed to customers in Utah.
Who is at risk
Anyone who consumed this product could be at risk, especially people with weakened immune systems, young children, or the elderly.
What to do
If you purchased Aonic Complete Hers in Utah, stop using it immediately and do not consume it. Contact Aonic Inc. or your retailer about returning the product, and contact your doctor if you experience symptoms like nausea, vomiting, diarrhea, or fever.
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.
Quantity affected
3630 individual bottles
Distribution
Distributed to customer in Utah.
Lot / code info
Lot 5349A BB 12/27; Lot 5363A BB 12/27
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recalling firm
TKS Co-pack Manufacturing, LLC
2642 W 400 N Ste 700
Lindon, UT 84042-1142
United States
Recall classification
Remote probability of serious adverse health consequences, or temporary reversible consequences.