Turmeric Capsule Recall: Qunol Extra Strength 1000 mg
Announced 2026-02-04 · FDA
The FDA is recalling Qunol Extra Strength Turmeric Capsule 1000 mg due to mold contamination detected in raw material lots produced in July and used in finished goods. The recall covers 60-count vegan and 120-count vegan bottles and includes several lot/part numbers distributed to multiple states.
| Brand | QUTEN RESEARCH INSTITIUTE LLC |
|---|---|
| Product | Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle . |
| Reason | Mold contamination detected for raw material lots that were produced in July and used in finished goods. |
| Severity | moderate |
| Units affected | 1000 |
| Distribution | The product was distributed to the following states: TX, FL, CA, NC, MI, MN, VA, NJ, MA, OH, IL,AL, CT, TN, NY, MO, PA, RI, SC, OK, GA, MN, WI, NV, IN, IA, CO, LA, NC, OR, KY, DE, |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use the recalled product and set it aside.
- Check your bottle for the recall lot/part numbers and packaging, and stop using if it matches.
- Contact the retailer or manufacturer for disposal or reimbursement instructions.
- If you have health concerns, consult a healthcare provider.
How to identify the recalled item
| Lot / date codes | Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281 |
|---|---|
| Lot / date codes | Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281 |
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.