---
title: "Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink s... — FDA record H-0520-2026 | Is It on Recall"
description: "Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination."
url: https://isitonrecall.com/recall/fda-food-h-0520-2026-aonic-complete-hers-dosage-single-serving-liquid-dietary-supplement-drink-shot-34-ml-1-1-fl-oz-in-pl/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle... — FDA record H-0520-2026

Reported completed

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 15, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
- **Classification**: Class II
- **Recalling firm**: TKS Co-pack Manufacturing, LLC
- **Quantity**: 3630 individual bottles
- **Agency-reported status**: Completed
- **Source record identifier**: H-0520-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0520-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot 5349A BB 12/27; Lot 5363A BB 12/27 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Distributed to customer in Utah.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Utah](https://isitonrecall.com/state/utah/)

## Dates in the source

- **Report date**: Feb 18, 2026
- **Recall initiation date**: Jan 15, 2026
- **Center classification date**: Feb 20, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0520-2026%22)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [TKS Co-pack Manufacturing, LLC records](https://isitonrecall.com/brand/tks-co-pack-manufacturing-llc/)