Vita Warehouse Corp. Three Gummy products in the famous vitamin B12 due to the capabilities Unnamed peanut pollutionAmerican Food and Drug Administration (FDA(Announced this week.
Newsweek I arrived at Vita Warehouse Corp on Saturday to comment.
Why do it matter
Individuals with allergies to peanuts have immune systems that interact with peanuts, with symptoms that may include skin reactions, itching or tingling in the mouth or throat, digestive problems such as diarrhea, liquid nose, throat and breathing.
In severe cases, people with food allergies may go to allergies – peanuts are the most common cause of allergic reactions.
Excessive sensitivity may have difficulty breathing, swelling of the lips, tongue and throat, low blood pressure, rapid pulse, dizziness, tulips or loss of consciousness.
American Food and Drug Administration/Food and Drug Administration
What do you know
The affected products include three distinctive combinations of vitamin B12:
- Welby’s 1000 McG 140-Count Gummies in green, red, white and packaging (UPC: 4099100290868);
- Berkley Jensen’s 1000 McG 250-Count Gummies in red and pink (UPC: 888670132487)
- Vitaglobe additional 60 currencies with white and red packages (UPC: 850005214670)
All products are characterized by clear bottles with white covers, with many symbols and expiration dates printed on the bottle bottom. No diseases or allergic reactions have been reported yet.
Consumers must check these details before use, as products with a large number of appointments are affected by 248046601 and October 2026.
The recalling process extends multiple distribution channels, including Aldi and BJ material sites at the country level, as well as online sales through the company’s sites and Amazon.
Vita Warehouse Corp. confirmed. There are no other products under these commercial names affected by the summons.
What people say
Vita Warehouse Corp: “This voluntary summons started with an abundance of caution to ensure consumer safety and confidence. We are committed to maintaining the highest standards of safety and quality of the product.”
In an e -mail message to Newsweek In January, the FDA said: “Most of the calls are voluntarily carried out by the product manufacturer, and when the company issues a general warning, usually by the news statement, to inform the public of the volunteer product, the FDA participates in our website as a public service.
“The role of the FDA (FDA) during a voluntary summons and began in the company is to review the summons strategy, assess the health risks offered by the product, monitor the summons, and the public sofas and other companies in the supply chain on the summons,” the Food and Drug Administration (FDA) continued.
He added: “The FDA (FDA) provides access to the public to information about retrieval operations by publishing a retrieval list according to its classification in the Food and Drug Administration enforcement report, including the specific action taken by the company K.
American Food and Drug Administration/Food and Drug Administration
What happens after that
Consumers who bought the affected products immediately stop using them and return the elements to the purchase place for their full recovery or get rid of them safely. Those who suffer from allergic reactions should search for immediate medical attention.
I created Vita Warehouse Corp. A hotline for consumers on the number 1-855-214-0100, which works from Monday to Friday from 7:30 am to 4:00 pm EST, to address customer and concerns questions.
