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A brand of cheeseburgers is recalled due to undeclared allergens.
Sheehan Brothers before made a voluntary reminder For its cheeseburgers, which have been distributed in three states, due to undeclared sesame.
Consequently, the Food and Drug Administration (FDA) has classified the recall as a class I health risk, the most serious type of recall.
Why it matters
According to the FdaMillions of people in the United States have food allergies or food sensitivities. Food sensitivities can go from light to potentially potentially deadly symptoms. The agency recognizes nine main food allergens: milk, eggs, sesame, fish, trees, crustaceans, peanuts, wheat and soy.
Press Association / AP
What to know
In addition to the cheeseburgers, the company also remembers its spicy chicken sandwich, its Italian mini-man, pizza of pepperoni, his chili cheese cone and rible-barbe riblet with a hard cabbage salad with unsuccessful sesame.
All products have received a class I health risk.
A Class I health riskAs defined by the FDA, is published when there is a reasonable probability that the use or exposure to a product will result in serious unfavorable consequences for health or death. This designation indicates that the product represents an immediate danger to public health and requires urgent attention from consumers and health professionals.
The affected products have been distributed in Indiana, Kentucky and Ohio, in particular by micro-markets and automatic distributors located throughout Ohio, northern Kentucky and East Indiana. They were available for purchase between July 2 and 8, 2025.
The problem was identified during a routine inspection led by the Ohio Ministry of Agriculture. Although no illness has been reported in relation to the elements recalled, people with an allergy to sesame or serious sensitivity are at the risk of undergoing a serious or potentially deadly allergic reaction if they consume the product.
All affected products have been wrapped in plastic.
What people say
The FDA, in an email at Nowsweek In January: “Reminders in the United States are voluntarily made by the manufacturer of products and when a company issues a public warning, generally by press release, to inform the public of a voluntary product reminder, the actions of the FDA which publish on our website as a public service.
“The role of the FDA during a voluntary reminder and initiated by the company is to examine the recall strategy, to assess the danger to the health presented by the product, to monitor the recall and, as an appropriate Alerte, the public and the other companies of the supply chain on the reminder.”
He added: “The FDA provides public access to information on reminders by publishing a list of reminders according to their classification in the FDA application report, including the specific measures taken by the Recall Company. The FDA application report is designed to provide a public list of products on the market which are recalled.”
What happens next
Consumers who suffer from an allergy or a sensitivity to sesame are invited to immediately eliminate the affected product and to contact Sheehan Brothers delivering to receive a replacement pack. Anyone who feels signs or symptoms of a disease of food origin or an allergic reaction should consult a doctor quickly.
