QUTEN RESEARCH INSTITIUTE LLC Recall: Mold contamination detected for raw material lots that were produced in July and used in finished goods.
United States
OngoingClass II
- Company
- QUTEN RESEARCH INSTITIUTE LLC
- Product
- Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle…
- Recall date
- December 16, 2025
- Source
- FDA
Reason for recall
Mold contamination detected for raw material lots that were produced in July and used in finished goods.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle . | Not published in this source record | Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160 | Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281 |
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
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0418-2026
- Event ID
- 98211
- Status
- Ongoing
- Classification
- Class II
- Company
- QUTEN RESEARCH INSTITIUTE LLC
- Product description
- Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count bottle ,BIO8281 60 count bottle .
- Quantity
- Turmeric 1000mg Capsule 60ct Veg., 3276, Turmeric 1000mg Capsule, 120ct Veg. BJ ,10304, Turmeric 1000mg Capsule 120ct Veg. 29160
- Reason
- Mold contamination detected for raw material lots that were produced in July and used in finished goods.
- Recall initiation date
- December 16, 2025
- Report date
- February 4, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- 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,
- UPC, lot, and code information
- Part Number Lot 12811C120 BIO7771 12811C120BJ BIO7772 12811C60 BIO8281
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: QUTEN RESEARCH INSTITIUTE LLC
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Texas | 1 |
| Florida | 1 |
| California | 1 |
| North Carolina | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Virginia | 1 |
| New Jersey | 1 |
| Massachusetts | 1 |
| Ohio | 1 |
| Illinois | 1 |
| Alabama | 1 |
| Connecticut | 1 |
| Tennessee | 1 |
| New York | 1 |
| Missouri | 1 |
| Pennsylvania | 1 |
| Rhode Island | 1 |
| South Carolina | 1 |
| Oklahoma | 1 |
| Georgia | 1 |
| Wisconsin | 1 |
| Nevada | 1 |
| Indiana | 1 |
| Iowa | 1 |
| Colorado | 1 |
| Louisiana | 1 |
| Oregon | 1 |
| Kentucky | 1 |
| Delaware | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
