King’s Hawaiian is voluntarily recalling its Pretzel Slider Buns, Pretzel Hamburger Buns and Pretzel Bites products out of an abundance of caution following a recall of an ingredient used in the pretzel products from one of its suppliers, Lyons Magnus. Lyons Magnus is recalling this ingredient due to the potential for it to cause microbial contamination including from the organisms Cronobacter sakazakii and Clostridium botulinum. While no illnesses associated with King’s Hawaiian pretzel bread have been reported, and no pathogens have been found in any King’s Hawaiian products to date, the recall is being conducted to ensure consumer safety.
This recall does not impact any other King’s Hawaiian products, as no other products use this ingredient from Lyons Magnus. King’s Hawaiian will resume producing all pretzel products once the company has ensured all current product has been disposed of and has confirmed the safety of all ingredients.
Consumers in possession of any King’s Hawaiian Pretzel Slider Buns, King’s Hawaiian Pretzel Hamburger Buns or King’s Hawaiian Pretzel Bites should dispose of the product. Consumers can contact King’s Hawaiian at 877-695-4227, Monday through Friday from 8:30 a.m. to 5:00 p.m. PT, if they have any questions, or to request replacement product.
King’s Hawaiian advises that consumers in possession of any King’s Hawaiian Pretzel Slider Buns, King’s Hawaiian Pretzel Hamburger Buns or King’s Hawaiian Pretzel Bites should dispose of the product.
Additional information including lot codes and product photos is available at: King’s Hawaiian® Issues Voluntary Recall of Pretzel Slider Buns, Pretzel Hamburger Buns and Pretzel Bites Due to the Recall of an Ingredient from Supplier Lyons Magnus | FDA
The Gluten Free Bar of Grand Rapids, MI is issuing a voluntary recall on The GFB 1.2 oz Dark Chocolate Coconut Bites because it may contain a potential undeclared allergen, cashew. People who have any allergy or sensitivity to cashew run the risk of serious or life-threatening allergic reaction if they consume these products.
The retail unit is in a 1.2 oz. wrapper (UPC 856818008895) with lot code 041323-174 printed on the back of the wrapper. Photos of the product and lot code are shown below. This recall is limited exclusively to the product and lot code listed, no other products are affected by this recall.
The recalled 1.2 oz Dark Chocolate Coconut Bites were distributed nationwide in retail stores and through online retailers as well as at www.thegfb.com.
The recall was initiated after it was discovered that the product potentially contained cashews from an isolated incident and was distributed in packaging that did not declare cashews. To date, one allergic reaction has been reported.
Consumers who have purchased The GFB 1.2 oz Dark Chocolate Coconut Bites with lot code 041323-174 are encouraged to return them to the place of purchase for a full refund. Consumers with questions may contact The Gluten Free Bar at 616-755-8432 Monday - Friday 9am – 5pm EST.
Additional information and product photos are available at: The Gluten Free Bar Issues Allergy Alert on Undeclared Cashew in The GFB 1.2oz Dark Chocolate Coconut Bites | FDA
Kraft Heinz is announcing a voluntary recall of approximately 5,760 cases of Capri Sun Wild Cherry Flavored Juice Drink Blend beverages.
The voluntary recall comes after diluted cleaning solution, which is used on food processing equipment, was inadvertently introduced into a production line at one of our factories. Only the Wild Cherry flavored Capri Sun products with the case/package information below are affected.
The “Best When Used By” date on the products is June 25, 2023.
The issue was discovered after we received several consumer complaints about the taste of the affected product. The Company is actively working with retail partners and distributors to remove potentially impacted product from circulation.
Consumers who purchased these items should not consume the product and can return it to the store where it was purchased. Consumers can contact Kraft Heinz from 9 a.m. to 6 p.m. Eastern Standard Time, Monday through Friday, at 1-800-280-8252 to see if a product is part of the recall and to receive reimbursement.
Kraft Heinz is committed to upholding the highest safety and quality standards.
Additional information including lot codes and product photos is available at: Kraft Heinz is announcing a voluntary recall of Capri Sun Wild Cherry Flavored Juice Drink Blend Beverages Due to Potential for Chemical Contaminants | FDA
Lyons Magnus LLC (“Lyons Magnus” or the “Company”) today announced that following continued collaboration and consultation with the U.S. Food and Drug Administration (“FDA”) and in furtherance of its longstanding commitment to food safety, the Company is expanding its July 28, 2022, voluntary recall of nutritional and beverage products to include additional brands and code dates. A complete list of the recalled products is in the table below. Consumers also are advised not to consume any products that are beyond their Best By Date.
This recall is being conducted due to the potential for microbial contamination, including from the organisms Cronobacter sakazakii and Clostridium botulinum. Although Clostridium botulinum has not been found in products, consumers are warned not to consume any of the recalled products even if they do not look or smell spoiled. The list of recalled products does not include products intended for infants (i.e., under the age of one).
While infection related to Cronobacter sakazakii is rare, the common symptoms of illness could include fever, vomiting and urinary tract infection. However, vulnerable and immunocompromised populations may be more susceptible to infection.
Clostridium botulinum may cause a severe form of food poisoning. It can begin from six hours to two weeks after eating food that contains the toxin. Symptoms may include double vision, blurred vision, drooping eyelids, slurred speech, difficulty swallowing, and muscle weakness. Botulism poisoning can cause respiratory paralysis, resulting in death, unless assistance with breathing (mechanical ventilation) is provided.
Root cause analysis indicates that the products did not meet commercial sterility specifications.
The products are packed in various formats under many different brand names, which are listed in the table below. To identify the Lot Code and Best By Date refer to the top of the carton for individual cartons or the side of the case for multi-carton cases. Some products were distributed nationally, while some products were limited in scope. Products included in the recall were distributed starting in April 2021.
Anyone who has a recalled product in his or her possession should dispose of it immediately or return it to the place of purchase for a refund. Consumers in all time zones with questions may contact the Lyons Recall Support Center 24/7 at 1-800-627-0557, or visit its website at www.lyonsmagnus.com. This recall is being conducted in cooperation with the FDA.
The recalled products are*:
*Bolded items denote additional brands, products and lots introduced in the expanded recall.
About Lyons Magnus
A leader in the food industry, Lyons Magnus produces and markets a wide array of products for the global foodservice and food ingredient channels. Lyons Magnus’ expertise includes a robust product development platform and the ability to commercialize both custom formulations and premium Lyons brand products.
Media Contacts
Andy Brimmer / Aaron Palash
Joele Frank, Wilkinson Brimmer Katcher
+1 212-355-4449
Additional information including lots codes and product photos is available at: Lyons Magnus Expands Voluntary Recall to Include Additional Nutritional and Beverage Products Due to the Potential for Microbial Contamination | FDA
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