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 |
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.
How to identify the recalled item
| Lot / date codes | Lot 5349A BB 12/27; Lot 5363A BB 12/27 |
|---|---|
| Lot / date codes | Lot 5349A BB 12/27; Lot 5363A BB 12/27 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
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.