If you take this for your allergies, stop immediately, the FDA warns
Use could have "severe or deadly" results.
Across the country,Allergies are a widespread affliction. More ... than50 million Americans Discover various types of allergies each year, depending on the ASTHME and America allergies Foundation (AAFA). This means that households across the United States rush to remedies when the symptoms light up. But if you recently bought a cure for allergies, read the rest to learn important recall information that could affect your home products now.
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Seasonal allergies affect approximately 24 million Americans each year.
According to published AAFA data, around 24 million people in the United States have been diagnosed withSeasonal allergic rhinitis, better known as hay fever in 2018 only. This is about 8% (19.2 million) adults and 7% (5.2 million) of children. Symptoms of these types of allergies can increase trees, herbs and weeds in response to pollen, and can be reduced by over -the -counter remedies.
Buzzagogo recalls a remedy against allergies distributed in the country in stores and online.
Buzzagogo Inc., based in New Hampshire, based in New Hampshire, voluntarily remembers a large number of his allergic bees disappeared for children of nasal remedy. The recall is carried out with the knowledge of the Food and Drug Administration of the United States (FDA), which published the companyrecall alert On June 7, the same date as it was announced.
The product is intended to improve the symptoms of seasonal allergies and is packed in individual tubes for a topical nasal application. The affected allergic bee has disappeared for children of nasal swab remedy is 2006491 with an expiration date in August 2024 and an UPC code of 860002022116. These two identification numbers are specified at the bottom of the product cardboard. This lot was distributed across the country to wholesale distributors, retail and online stores on the company's website, as well as Amazon.
The remedy for children's allergies could be marred by dangerous contaminants.
The reason for the recall is that the products have the potential for microbial contamination: FDA tests have revealed that some contain high levels of yeast and mold, as well as the potential to contain bacteria Bacillus cereus.
In immunocompromised patients, the use of the affected product could potentially lead to "severe or deadly adverse events", such as bacteremia / septicemia, pneumonia, invasive fungal rhinosinusitis or disseminated fungal infection, according to the recall alert .
Even in non -immunocompromised patients, the use of recalled products could cause infectious complications, such as bacteremia or non -invasive fungal rhinosinusitis. But in these more healthy populations, reactions are more likely to be less serious and more sensitive to treatment.
Fortunately, at this stage, Buzzagogo has not received any complaints linked to microbial concerns or the reports of adverse events linked to this lot recalled.AE0FCC31AE342FD3A1346EBB1F342FCB
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Here is what to do if you have one of the allergy products recalled at home.
Buzzugogo currently informs its distributors and customers by e-mail and organizes the return or replacement of all the products recalled. The reminder notice advises customers (as well as distributors or retailers) who have allergy to the allergy that has disappeared for children with nasal swab with the 2006491 lot number to stop using the product immediately. Throw away any remaining product and contact the company [email protected] For a full refund. "We are looking to minimize all the drawbacks that this can cause consumers and we are engaged in their total satisfaction," said the declaration of the company.
Consumers with questions concerning this recall can contact Buzzagogo by phone at 800-963-2861 or by e-mail [email protected] Monday to Friday from 9 a.m. to 5 p.m. EDT.
If you think you have encountered problems that can be linked to the use of this product, immediately contact your doctor or health care provider.
You can also report adverse reactions or quality problems related to the product MEDWATCH FDA MEDWATCH on line. You can also do by ordinary or fax by first by first Download the report form (or call the 800-332-1088 to request one), then finish it and return it to the address on the pre-treatment form or by fax to 800-FDA-0178.
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