Dietary supplement drink Recall: Aonic Complete Hers
Announced 2026-02-18 · FDA
The FDA is recalling 780 bottles of Aonic Complete Hers, a single-serving liquid dietary supplement drink shot, 34 ml, distributed to Utah, due to possible contamination with coliforms, E. coli, and/or Pseudomonas aeruginosa. The recall involves Lot 5349A BB 12/27 and Lot 5363A BB 12/27.
| Brand | TKS Co-pack Manufacturing, LLC |
|---|---|
| Product | 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. |
| Reason | Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. |
| Severity | moderate |
| Units affected | 3630 |
| Distribution | Distributed to customer in Utah. |
| Agency | FDA |
| Recall / campaign no. | Lot 5349A BB 12/27; Lot 5363A BB 12/27 |
WHAT YOU SHOULD DO
- Do not consume the product.
- If you have any of the affected lots (5349A BB 12/27 or 5363A BB 12/27), discard it or return it to the place of purchase for a refund or replacement.
- Contact the retailer or manufacturer for disposal instructions or a replacement/refund.
- If you have consumed the product and feel unwell, seek medical advice.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.