FDA Recalls Butter Due to Undeclared Allergen

The FDA has issued a Class II recall for 64,800 pounds (1,800 cases) of NH European Style Butter Blend manufactured by Bunge North America Inc. This recall affects both the United States and the Dominican Republic.

Why Was the Recall Initiated?

The recall was initiated due to an undeclared allergen in the butter blend, specifically milk. The FDA's action highlights the importance of stringent quality control measures in food production.

Impact on Consumers

More than 64,000 pounds of butter have been recalled across these two countries. While it is not yet clear if anyone has been harmed by this issue, recalls like these underscore the need for consumers to be vigilant when purchasing food products.

What Consumers Should Do

If you purchased any of the recalled butter blends, Bunge North America Inc. advises contacting them directly at 1-800-BUNGE-North (1-800-286-4563) or visiting their website for further instructions on what to do next.

Additional Information

The FDA has provided detailed information about the recall, which can be found on their official website. It's important for consumers and food industry professionals alike to stay informed about such recalls to ensure public safety.