← FDA ENFORCEMENT
H-0520-2026Class II

TKS Co-pack Manufacturing, LLC

Recalling firm
TKS Co-pack Manufacturing, LLC
Product type
Food / supplement / cosmetic
Status
Completed
Report date
2026-02-18
Distribution
Distributed to customer in Utah.
Firm state
UT
Product quantity
3630 individual bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

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.

Code / lot info

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

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.