Severity
Moderate
ModerateClass IICompleted
FDA Food recall · Reported February 18, 2026
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.
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Tks Co-pack Manufacturing, LLC recalled Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (… - a moderate-severity action.
Aonic Complete Hers. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (… was recalled by Tks Co-pack Manufacturing, LLC in February 18, 2026. Reason: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.. Check the official notice for the remedy. Verify recall #H-0520-2026 with the FDA Food before acting.
The recall
Tks Co-pack Manufacturing, LLC issued this moderate-severity FDA Food recall-Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination..
- Moderate
- severity level
- Class II
- classification
- February 18, 2026
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-0520-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-0520-2026) was formally reported on February 18, 2026, with the manufacturer initiating the action on January 15, 2026. It is classified under Moderate severity (Class II), with a current status of Completed. Tks Co-pack Manufacturing, LLC is listed as the recalling firm, operating out of Lindon, UT. Federal records list the affected scope as 3630 individual bottles.
The documented reason for this recall is: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. Distribution data in the federal record shows the product reached: Distributed to customer in Utah.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
3630 individual bottles
Related Recalls
6
0 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | H-0520-2026 |
| Date reported | February 18, 2026 |
| Date initiated | January 15, 2026 |
| Recalling firm | Tks Co-pack Manufacturing, LLC |
| Firm location | Lindon, UT |
| Affected scope | 3630 individual bottles |
| Distribution | Distributed to customer in Utah. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (H-0520-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Tks Co-pack Manufacturing, LLC. Units affected: 3630 individual bottles.
Why was this product recalled? ▼
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on February 18, 2026. Severity: Moderate. Recall number: H-0520-2026.
Where was the recalled product distributed? ▼
Distribution: Distributed to customer in Utah..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-0520-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported February 18, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.