The bread recall due to undeclared milk in some products affects stores in Hawaii.
The Food and Drug Administration has classified a batch of bread rolls produced by Jesse's Bakery, Inc. in Honolulu, Hawaii, at its highest risk level, Class I, after the company recalled the product in February due to undeclared milk.
This classification indicates that consuming the affected product could result in serious adverse health consequences or even death.Newsweek contacted Jesse's Bakery via voicemail for this story.Why It MattersThe products contained undeclared milk, which is one of the nine main allergens in the U.S. The FDA said that while most symptoms from food allergies are mild, some may progress to severe, life-threatening allergic reactions called anaphylaxis.It also said that this can cause people to suffer constricted airways in the lungs, severe lowering of blood pressure and shock, and suffocation by swelling of the throat and larynx.What To KnowThe recall was triggered by the presence of undeclared milk in the Pan de Sal product.Allergic reactions to milk can range from mild symptoms, such as hives or gastrointestinal distress, to severe anaphylactic reactions that require immediate medical attention.Jesse's Bakery, Inc. voluntarily initiated the recall on February 7, 2025, following internal quality checks. The FDA classified the recall as a Class I event on March 4, 2025, signaling the highest level of concern for public health.The recalled Pan de Sal is packaged in a 9-ounce flexible poly bag containing six rolls. The product label includes the branding for Jesse's Bakery, Inc., along with its Honolulu address and contact information. The affected items bear the UPC code 0 38511 00703 4 and may include one of the following product codes: 26, 206, 27, 207, 28, 208, 29, 209, 210, 211, 212, 213, and 214.A total of 97 Spanish roll packages are included in the recall, with distribution limited to Hawaii. The bakery has not yet issued a public press release regarding the recall.What People Are SayingAccording to the FDA website, the agency issues a Class I recall in 'a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.'What Happens NextAt time of writing, the FDA does not have a termination date scheduled for the recall to end.Do you have a story we should be covering? Do you have any questions about this article? Contact LiveNews@newsweek.com.
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