A nationwide recall has been issued for certain NuNaturals sweetener products due to a significant labeling error. The U.S. Food & Drug Administration (FDA) has classified this recall as a Class II risk, indicating a potential for temporary or medically reversible adverse health consequences, though the risk of serious harm is considered remote.
What's the Issue?
NuNaturals, Inc. voluntarily recalled specific lots of its Organic Pure Stevia and Pure Monk Fruit Sweetener on July 14th after discovering that some products were mislabeled. Bottles labeled as Organic Pure Stevia actually contained Monk Fruit powder, while those labeled as Pure Monk Fruit Sweetener contained Stevia powder.
Which Products Are Affected?
The recall involves a total of 156 bottles: 78 bottles of Organic Pure Stevia and 78 bottles of Pure Monk Fruit Sweetener. Both products were distributed to retailers nationwide. Here are the specific details to check:
- Organic Pure Stevia - 1 oz:
- UPC: 7 39223 00204 0
- Lot number: 25104S
- Best By: April 2028
- Packaged in a plastic bottle
- Pure Monk Fruit Sweetener - 0.71 oz:
- UPC: 7 39223 00187 6
- Best By: April 2028
- Packaged in a plastic bottle with white cap
What Should You Do?
The FDA and NuNaturals advise consumers to stop using the recalled sweetener products immediately and discard them. While the risk is considered low, it's important to avoid any potential adverse reactions due to the mislabeling.
Why is this a Class II Recall?
According to the FDA, a Class II recall means that using or being exposed to the mislabeled product could lead to temporary or medically reversible health issues. However, the likelihood of serious adverse health consequences is considered remote.
Stay Informed
It remains unclear what caused the labeling error, and NuNaturals has not yet commented on whether any consumers have been affected. Stay tuned for updates as more information becomes available.