Good Lifestyle

There are a lot of rules and regulations in place to keep potentially dangerous foods , drinks and drugs out of the market in the United States. However, security surveillance does not stop after distributing a product to stores and retailers. Agencies like Food & Drug Administration (FDA) keep an eye on all articles that may have a public health risk even after their path on the shelves. And now, the FDA has issued reminders on several products, including seafood, mushrooms, condiments and eye ointments. Read the rest to find out more about the latest batch of agency announcements.

Read this then: Popcorn sold in 9 states recalled on health problems, warns the FDA .

On February 26, the FDA announced that New York Kawasho Foods USA had voluntarily recalled cans of his medium shrimps of Geisha sold in cans of 4 ounces. The articles affected were sent to the department stores of California, UTAH, Arizona and Colorado, including Walmart, Associated Foods, Stater Bros Markets, Safeway and Albertsons. Customers can identify the seafood recalled by checking the cans for the UPC 071140003909, the LGC12W12E222222222 and the date of May / 12/2026 of the Lot code, printed at the bottom of the package.

The company warns that it has received reports on the cans recalled "swelling, fleeing or bursting". This could mean that the element has been subcontracted, "which could lead to the potential of deterioration organizations or pathogens." Customers are advised not to eat the product - even if it does not seem to show signs of deterioration and return it to its place of purchase for a full refund.

Mushrooms can be a crucial ingredient in everything, from soups to accompanying dishes, but you may want to check what is in your refrigerator if you recently buy it. The FDA announced on February 24 that California Jan Fruits Inc. had recalled all cases of its Enoki mushrooms in 200g / 7.05 oz packages. The company says that the affected product was sent to "small distributors of local products or wholesalers" in California for an additional distribution to retailers across the State, as well as in Hawaii.

The affected mushrooms are sold in a transparent plastic set with the description "Taiwan Best Quality Enoki Natural Mushroom *** Manufacturer: Changhua County Champlems Cooperative Production" Printed in English. Customers can also look for the UPC 851084008358 at the back of the product and the word "premium" printed in green alongside two QR scan codes.

The company said it had drawn the product after sampling of routine carried out by Hawaiian officials have returned positive for Listeria monocytogenes . The agency warns that dangerous bacteria usually cause short -term symptoms in most people, such as "high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea". However, microorganism can cause potentially fatal infections in young children, the elderly or any immunocompromised person. This can also lead to false layers and mortinagers for those who are pregnant. AE0FCC31AE342FD3A1346EBB1F342FCB

The company says that it has so far "stopped the production and distribution of the product when we continue our investigation into what caused the problem". Customers are advised to return the article assigned to their place of purchase for a full refund.

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On February 22, the FDA announced that Pennyslvania Sunny Dell Foods, LLC had recalled 12 ounce pots from its brand roasted red pepper house with Portobello mushrooms. The company says it has distributed the product in retail stores across the northeast of the United States and customers through orders by mail placed online.

Customers can identify the affected pots by locating the SD21160-03 RPOA Lot code printed in addition to its ceiling and the UPC 747479001106. The company has specified that no other batch of product - or any other soup or sauce sold under The Homemade de Rao brand - is not affected by the recall.

According to the opinion of the FDA, the company withdrew the product from the shelves after discovering that it could contain uncommented gables. The known food allergen is classified as a tree nut, the agency warning that any allergic person or a severe sensitivity to the ingredient "run the risk of a serious or fatal allergic reaction if they consume these products".

After an investigation, the company said that it had discovered a labeling error which meant that the packed pots like roasted peppers and Portobello mushrooms actually contained a condiment which contains trees. Customers can receive a full refund by returning the product to the store where it was purchased.

It is not only food products that have recently been scandal in one of the agency's announcements. On February 24, the FDA announced that Global Pharma Healthcare Had voluntarily recalled part of his artificial eye ointment distributed by Delsam Pharma. The company claims that the product is used "as a lubricant for the eyes and to relieve the dryness of the eyes" and contains mineral oil of 15% and white essence 83% as an ingredients listed. The assigned item is packed in white aluminum tubes sold in a white paper card, both printed with the NDC 72570-122-35 and UPC 3725700122353.

The company says it has drawn the product "due to possible microbial contamination", adding that items may have a damaged leak or packaging. The opinion warns that the use of the recalled ointment "can cause undesirable events, including an infection in the eye that could lead to blindness".

According to the agency's opinion, customers who bought the recalled ointment are invited to stop using it immediately and to throw it "in complete safety and appropriately". Anyone who believes he has developed health problems using the product must contact his doctor or health care provider as soon as possible.

The last reminder comes a few weeks after Global Pharma Healthcare published a previous reminder for 10 different brands of Artificial tears eye drops . The FDA and the Centers for Disease Control and Prevention (CDC) said that a joint survey had connected the products to one " largely resistant to drugs "Stump of Pseudomonas aeruginosa bacteria. As the recall was announced on February 1, agencies reported that 55 patients in 12 states had been infected, signaling symptoms such as eye inflammation, respiratory infections, urinary tract infections and sepsis.