FDA Food · 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.

Class II · Completed

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

Affected lots / codes — check yours against thisLot 5349A BB 12/27; Lot 5363A BB 12/27

Recalling firm: TKS Co-pack Manufacturing, LLC, Lindon, UT
Classification: Class II (temporary or reversible harm possible)
Status: Completed
Quantity: 780 individual bottles
Distribution: Distributed to customer in Utah.
Recall initiated: January 15, 2026
Classified: February 20, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0521-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

Check this brand across all 8 databases →