Food and Beverage Recalls
Enoki King Mushroom Farm recalls Enoki King Enoki Mushroom 5.3 oz
Enoki King Mushroom Farm Recalls Enoki Because of Possible Health Risk
FOR IMMEDIATE RELEASE - Enoki King Mushroom Farm of Ventura, CA is recalling lot 4877 of its 5.3-ounce (150g) packages of Enoki Mushroom (Product of USA) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled Enoki comes in a clear plastic package with the description “Enoki Mushroom” in English and French with the lot code, 4877, on the front in black ink. At the back, there is UPC code 860011505600. The products were distributed from CA and NY through produce distributors or wholesalers to retail stores nationwide.
No illnesses have been reported to date in connection with this problem.
Reser’s Fine Foods recalls Bistro 28, Don Pancho Meal kits containing chicken
Out of an abundance of caution, Reser’s Fine Foods is voluntarily recalling a limited number of meal kits due to the inclusion of recalled chicken from an outside ingredient supplier (BrucePac). The ingredient supplier (BrucePac) recall is due to possible Listeria monocytogenes contamination.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Tipical Latin Food Corp. recalls Los Andes Foods Cachapa de Maiz sweet corn pancakes
Tipical Latin Food, Corp. Issues Allergy Alert on Undeclared Wheat in Cachapa de Maiz
TIPICAL LATIN FOOD CORP of Miami, FL is recalling Cachapa de Maiz sweet corn pancakes labeled under Los Andes Foods, because it may contain undeclared wheat. People who have an allergy or severe sensitivity to run the risk of serious or life-threatening allergic reaction if they consume these products.
Cachapa de Maiz sweet corn pancakes was distributed to TRIMAR USA LLC in Miami, FL who further distributed the product to retail and wholesale customers. This product can be identified by the yellow label and the vacuum seal bag it comes in. Lot number for this product can be found at the bottom of the bag in a blue label and range from 2622404 to 2772412.
No illness has been reported to date.
Wismettac Asian Foods, Inc. recalls Shirakiku Korean Seasoned Seaweed
Wismettac Asian Foods Issues Allergy Alert on Undeclared Sesame in Seasoned Seaweed
Wismettac Asian Foods, Inc., Santa Fe Springs, CA is recalling 3.52 oz packages of Shirakiku brand Korean Seasoned Seaweed. The product contains the undeclared allergen of sesame on an outer package. People who have an allergy or severe sensitivity to sesame run the risk of serious or life-threatening allergic reaction if they consume those products.
The product was distributed in CA, AZ, TX, NM, WA, NY, NV through retail stores and resturants.
The product is packaged in a 3.52 oz, illustrated plastic bag, containing 5 inner packages. Each inner packages has the correct allergen information. The correct UPC for the product is 074410516031, located on the back right side of the outer package. However, the outer package has an incorrect allergen declaration due to the unintentional use of incorrect packing material, which also displays the wrong UPC: 074410495534.
No illnesses have been reported to date in connection with this issue.
Youngtown Grape Distributors Inc recalls Happy Moose Tropical Roots and Strawberry Fields, 12 oz bottles
Youngstown Grape Distributors Inc., a co-manufacturer for Happy Moose Juice, is voluntarily recalling Happy Moose Tropical Roots Juice (Lot# H240903-E BEST BY 12/02/2024) and Happy Moose Strawberry Fields (Lot# H240903-H, BEST BY 12/02/2024) because a portion of the production made did not complete the High Pressure Processing (HPP) treatment, which is used to prolong the product shelf-life, prevent spoilage, and significantly reduce the risk of pathogens such as Salmonella, Listeria monocytogenes and diarrheagenic E. coli. Those organisms could lead to serious illness if consumed.
It is important to note that there have been no reports of illness associated with these products to date. No other production codes or products are affected.
Medical Devices Recalls
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal, and Trilogy EV300 ventilators
- Additional Usage Instructions issued by Philips as voluntary correction (Urgent Medical Device Correction in the US, Field Safety Notice outside of the US)
- Additional Usage Instructions provide user action and guidance for continued use of affected devices
- Philips Respironics has not received any specific complaints of device malfunctions resulting from in-line nebulizer use; issue identified by retrospective review of flow sensor performance
Philips Respironics issued a voluntary correction for Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal, and Trilogy EV300 ventilators regarding the use of in-line nebulizers.
An Urgent Medical Device Correction (Field Safety Notice in the rest of world) is being sent to health systems and equipment distributors and is being communicated through this additional update to ensure patients who use the devices at home are informed in a timely manner.
Patients will receive communication from their usual health provider and should not discontinue therapy without consulting their healthcare provider. This update, and the associated Urgent Medical Device Correction (Field Safety Notice in the rest of world) provides instructions for user action and guidance for continued use of affected devices. Philips Respironics is investigating a solution and will provide additional information when available.
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