Independent recall-navigation resource • Verify urgent decisions with current FDA/company recall instructions.
FSFood Safety Notice
FDA source record

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.

Readable source details for FDA recall record H-0520-2026.

FDA recall number
H-0520-2026
FDA event ID
98325
Company
TKS Co-pack Manufacturing, LLC
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.
Classification
Class II
Status
Completed
Recall date
Feb. 18, 2026
Distribution
Distributed to customer in Utah.

Technical source

This page reformats the FDA enforcement record for readability. The original machine-readable record is available for verification.

View original openFDA data →