Full Breakdown
Qunol Turmeric Supplements Recall Due to Mold Contamination
2/8/2026, 9:56:08 PM
Overview of the Recall
The U.S. Food and Drug Administration (FDA) announced a Class II recall of approximately 42,740 bottles of Qunol Extra Strength Turmeric Capsules due to mold contamination. This recall, which affects 60- and 120-count bottles of 1,000-milligram capsules, was initiated by Quten Research Institute on January 23, 2026, following an initial recall in December 2025.
Identifying Affected Products
The recalled products include:
- Qunol Extra Strength Turmeric, 1000mg, 60-count bottle
- Product SKU: 300580
- UPC: 850184008428
- Lot code: B1O8281
- Expiration date: October 2028
- Qunol Extra Strength Turmeric, 1000mg, 120-count bottle
- Product SKU: 387443
- UPC: 850184008435
- Lot codes: B1O7771, BIO7772
- Expiration date: October 2028
These supplements were distributed to major retailers, including CVS and Walmart, across 30 states, including California, Florida, New York, and Texas.
Health Risk Classification
The FDA classified this recall as Class II, indicating a remote risk of serious health consequences. The classification suggests that while the risk is low, there is potential for temporary or medically reversible adverse health effects from consuming the contaminated products.
Consumer Guidance
Quten Research Institute advises consumers to stop using the affected turmeric capsules immediately. Customers who have purchased the recalled products are encouraged to return them to the retailer for a full refund. Retailers involved in the recall include CVS, Wegmans, and Walmart, among others.
Criticism & Opposition
While the recall aims to protect consumers, some critics have raised concerns about the frequency of contamination issues in dietary supplements. The FDA's oversight of supplement safety has been questioned, with calls for stricter regulations to prevent similar incidents in the future.
Official Statements
In a statement, Quten Research Institute emphasized the importance of consumer safety, urging anyone who has purchased the recalled products to act promptly. The FDA reiterated the need for vigilance regarding dietary supplements, highlighting the potential health risks associated with mold contamination.
Verbatim Quotes
- “Consumers should stop using the affected products and return them to retailers like CVS or Wegmans for full refunds.” — Quten Research Institute
- “The FDA classified the recall as Class II, meaning the supplements could cause temporary or medically reversible health effects.” — FDA Official Statement
What's Next
As the recall progresses, Quten Research Institute is expected to enhance its quality control measures to prevent future contamination incidents. The FDA may also review its regulatory framework for dietary supplements in light of this recall.
