A rapid recall has been issued for a batch of over-the-counter cold and flu medications widely available in the United States, due to potential contamination with animal waste, which could lead to the presence of Salmonella bacteria, according to “Newsweek.”
Gold Star Distribution has issued an urgent recall of all products regulated by the U.S. Food and Drug Administration (FDA) located at its headquarters in Minneapolis, after the agency discovered evidence of rodent feces, bird droppings, and other types of contamination.
The recall, which began on December 26, includes cold and flu medications, dietary supplements, food, pet food, cosmetics, and medical devices, primarily distributed in Minnesota.
According to the magazine, this broad recall affects a wide range of consumer health products at a time when the United States is experiencing a significant increase in cases of colds and flu.
Serious Defect:
According to the company’s statement, “People who handle or consume the products may become seriously ill as a result of contamination by pests, including rodents, birds, and insects.”
In this regard, an investigation by the U.S. Food and Drug Administration found that Gold Star Distribution’s facility was operating in conditions that did not adhere to health and safety standards, with specific risks associated with contaminated surfaces and airborne particles from animal waste.
The report revealed evidence of a serious defect in hygiene, including the presence of rodent feces and urine and bird contamination in storage areas.
This increases the risk of exposure to harmful microorganisms, posing threats such as Salmonella and Leptospira infections to a large segment of consumers, especially the most vulnerable groups, such as infants, the elderly, pregnant women, immunocompromised patients, and pets.
Gold Star stated: “Products stored in unsanitary conditions may be contaminated… Exposure to contaminated products may pose serious health risks to consumers, including the potential for bacterial contamination, which may lead to illness or infection, including Salmonella.”
It added: “Any side effects or problems related to the quality of this product can be reported to the FDA’s MedWatch Adverse Event Reporting program.”
