Latest news with #RelaxationTea
Newsweek
2 days ago
- Health
- Newsweek
Dessert Recalled Nationwide as FDA Issues Risk Warning
Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. The recall of cinnamon bun desserts produced by the Michigan-based Superior Foods Company has been given a Class II classification by the U.S. Food and Drug Administration (FDA) on Friday. The recall was in response to fears the desserts could have been contaminated with plastic. Newsweek contacted the Superior Foods Company for comment on Saturday via email outside of regular office hours. Why It Matters A Class II risk classification (one of three) refers to a situation in which the "use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote," according to the FDA. Foreign material contamination can potentially cause injury, and repeated incidents raise questions about the effectiveness of current safety protocols. Food recalls due to contamination or mislabeling can undermine consumer trust and place vulnerable individuals (such as children, the elderly, or those with allergies) at greater risk. What To Know The Superior Foods Company initially issued a nationwide voluntary recall for some of its 7-ounce packs of cinnamon bun desserts, sold under the Park Street Deli brand in plastic tubs, on July 24. On August 8, the product was given a Class II classification by the FDA. The recall covered 19,368 retail units. The recalled products have UPC number 4061462440151 and a sell by date of November 8, 2025. The FDA said a press release was not issued for the recall. This week, the agency also classified a voluntary recall of a macaroni and cheese snack, produced by Saint Louis based Louisa Food Products, Inc., as a Class II. The initial recall was issued on July 17 after a supplier conducted its own recall after discovering possible contamination with Listeria monocytogenes. On July 21, Los Angeles-based Herbalife International of America issued a voluntary recall for a consignment of its Relaxation Tea following an ingredients mix-up. This was categorized as a Class II recall by the FDA on August 6. Separately, DFA Dairy Brands, LLC has announced a recall of products produced by the Friendly's brand of Cookies & Cream ice cream in response to possible undeclared soy and wheat. Stock photograph showing a cinnamon bun in California on May 17, 2024. There is no suggestion that the bun pictured was impacted in any way by the Superior Foods Company product recall. Stock photograph showing a cinnamon bun in California on May 17, 2024. There is no suggestion that the bun pictured was impacted in any way by the Superior Foods Company product recall. Smith Collection/Gado/GETTY What People Are Saying On its official website, the Superior Foods Company said: "Built on the promise to ensure success for every single customer. Driven by the commitment to provide premium quality products and exceptional service. We are Superior Foods. For over 70 years, this dedication has not wavered as we continue to expand, seek out innovation, and push boundaries, all to be Superior for our customers." What Happens Next? The FDA will likely continue to monitor the Superior Foods Company product recall and will be looking out for any adverse health impacts, though none have been reported so far.
Newsweek
5 days ago
- Health
- Newsweek
Tea Recalled Nationwide as FDA Sets Risk Level
Based on facts, either observed and verified firsthand by the reporter, or reported and verified from knowledgeable sources. Newsweek AI is in beta. Translations may contain inaccuracies—please refer to the original content. A nationwide and cross-border recall of a popular relaxation tea, initiated after an ingredient mixup, has been designated by food inspectors as the second-highest risk level. Herbalife International of America, which is based in Los Angeles, issued a voluntary recall of its Relaxation Tea on July 21. The recall affects 5,888 products sold online across the United States as well as in Mexico and Ecuador. On August 6, the U.S. Food and Drug Administration (FDA) classified the recall as a Class II risk—a designation indicating products may cause temporary or medically reversible adverse health consequences. No press release was issued and the FDA's classification alert did not state which ingredients had been mixed up. Newsweek has contacted Herbalife via email outside of regular office hours on Thursday. Why It Matters The FDA's decision to classify the recall as a Class II risk signals a significant, though not life-threatening, potential for harm. Class II recalls address situations where the use of a product could cause temporary or medically reversible adverse effects, or the probability of serious consequences is remote. Stock image shows a woman smelling tea at sunset. Stock image shows a woman smelling tea at sunset. Getty Images What To Know The FDA said the recall stemmed from the use of an "incorrect ingredient received from supplier and used in manufacturing finished product Relaxation Tea." The items' lot code, which is often found near the product's bar code, is: D925507J02. The expiration date is 04/11/2027, the FDA alert said. Herbalife advised customers not to use the affected Relaxation Tea products. FDA inspectors assign recalls one of three classifications—Class I, Class II, or Class III—to indicate the degree of hazard to people's health. The classifications are defined by the agency as: Class I - 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. Class II - a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. Class III - a situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences. What Happens Next Consumers who purchased Herbalife Relaxation Tea are urged to check their packaging and discontinue use of any recalled units. Customers with affected products or safety concerns are advised to contact Herbalife's customer service or review the FDA's recall posting for detailed guidance.
