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

Get Real-Time Recall Alerts on Your Phone

Scan any grocery receipt and instantly know if your food has been recalled. Free download — protect your family in 3 seconds.