The U.S. Food and Drug Administration (FDA) has classified a recall of several coffee beverage powder products as a Class I recall, the agency’s most serious recall category, due to the potential presence of Salmonella contamination.
The recall was initiated by SKS Copack, a California-based manufacturer, and affects more than 600 bags of cappuccino and latte powder products distributed in New York and New Jersey.
Consumers are advised to check their products against the following recalled items:
Salmonella is a bacterium that can cause serious and sometimes fatal infections, particularly in young children, older adults, and individuals with weakened immune systems. Symptoms may include fever, diarrhea, nausea, vomiting, and abdominal pain. In severe cases, the infection can spread beyond the gastrointestinal tract and require hospitalization.
The FDA assigned the recall a Class I designation, indicating that there is a reasonable probability that consumption of the affected products could cause serious adverse health consequences or death.
Consumers who have purchased the affected products should not consume them. The recalled items should be discarded or returned to the place of purchase according to retailer instructions.
Anyone experiencing symptoms of Salmonella infection after consuming these products should seek medical attention promptly.
The FDA continues to monitor the recall and encourages consumers to stay informed about food safety alerts and product recalls.
