tks co-pack manufacturing, llcfoodHigh PriorityActive

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: t

tks co-pack manufacturing, llc 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: t was recalled by the FDA. Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

Plain-English Summary

tks co-pack manufacturing, llc 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: t was recalled by the FDA. Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source
FDA
Announced by source
January 15, 2026
Last reviewed by RecallRadar
March 4, 2026

What You Should Do

  1. 1## 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: t Agency: FDA | Category: food | Date: 2026-01-15 Reason: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. What to do:
  2. 2Stop using the product if it matches your lot/model.
  3. 3Compare your product details with the FDA recall notice.
  4. 4Follow the manufacturer's remedy instructions (refund, replacement, or disposal).
Open Official Recall NoticeGet Alerts for tks co-pack manufacturing, llc Devices

What's Being Recalled

Quoted source excerpt from the official notice.

Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Lot 5349A BB 12/27; Lot 5363A BB 12/27

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my tks co-pack manufacturing, llc device affected?

Check the affected models section on this page. The official notice currently lists Lot 5349A BB 12/27; Lot 5363A BB 12/27.

What is the remedy for this recall?

## 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: t Agency: FDA | Category: food | Date: 2026-01-15 Reason: Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination. What to do: 1. Stop using the product if it matches your lot/model. 2. Compare your product details with the FDA recall notice. 3. Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Keep browsing with these internal hubs: tks co-pack manufacturing, llc recall hub and Food & Drug recall hub.

Official Resources

Use these primary sources for final eligibility and claim instructions.

View official notice from FDA

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Quick Info

Brand
tks co-pack manufacturing, llc
Category
food
Source Agency
FDA
Announced
January 15, 2026
Country
US
Status
Active

Source & Verification

Sourced from FDA. Last reviewed March 4, 2026.

Official source
FDA
Announced by source
January 15, 2026
Last reviewed by RecallRadar
March 4, 2026

Official Resources

Use these primary sources for final eligibility and claim instructions.

Open Official Recall NoticeView official notice from FDA

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