MODERATE RISK
Completed
H-0521-2026
Aonic Complete His. 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. Sipping 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.
Recalled by TKS Co-pack Manufacturing, LLC
Classification
Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.
Reason for Recall
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Product Details
Product Quantity
780 individual bottles
Product Type
Food
Code Info
Lot 5349A BB 12/27; Lot 5363A BB 12/27
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Distributed to customer in Utah.
Company Location
Lindon, UT, 84042-1142
Timeline
Report Date
02/18/2026
Recall Initiated
01/15/2026
Classification Date
02/20/2026
Termination Date
N/A
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 28, 2026
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