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Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle .

quten research institiute llc Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle . was recalled by the FDA. Mold contamination detected for raw material lots that were produced in July and used in finished goods.

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

Plain-English Summary

quten research institiute llc Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle . was recalled by the FDA. Mold contamination detected for raw material lots that were produced in July and used in finished goods.

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
December 16, 2025
Last reviewed by RecallRadar
March 4, 2026

What You Should Do

  1. 1## Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle . Agency: FDA | Category: food | Date: 2025-12-16 Reason: Mold contamination detected for raw material lots that were produced in July and used in finished goods. 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 quten research institiute llc Devices

What's Being Recalled

Quoted source excerpt from the official notice.

Mold contamination detected for raw material lots that were produced in July and used in finished goods.

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281

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 quten research institiute llc device affected?

Check the affected models section on this page. The official notice currently lists Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281.

What is the remedy for this recall?

## Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle . Agency: FDA | Category: food | Date: 2025-12-16 Reason: Mold contamination detected for raw material lots that were produced in July and used in finished goods. 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: quten research institiute 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
quten research institiute llc
Category
food
Source Agency
FDA
Announced
December 16, 2025
Country
US
Status
Active

Source & Verification

Sourced from FDA. Last reviewed March 4, 2026.

Official source
FDA
Announced by source
December 16, 2025
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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