Recalls

No illnesses have been reported to date in connection with this problem.



The potential contamination was noted by a routine sampling conducted in the State of Missouri revealed the presence of Listeria monocytogenes in the 200g packages of “Enoki Mushrooms”.



The distribution of the product has been suspended while FDA and the company continue to investigate the source of the problem.



All Utopia branded Enoki Mushrooms imported from China and within expiry are effected by the recall. Consumers who have purchased the 200g packages of “Enoki Mushrooms” within expiry are urged to return them to the place of purchase for a refund.



Consumers with questions may contact the company at 718.389.8898 Monday-Friday EST 8AM-4PM.

The product being recalled is ByHeart Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12 Months in 24 oz containers. The formula under voluntary recall was distributed directly to consumers in the U.S. and can be identified by the number on the bottom of the can. Recalled product batches are 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1 printed with use by 01 JAN 24 or 01JUL 24.



Cronobacter bacteria can cause severe, life-threatening infections (sepsis) or meningitis (an inflammation of the membranes that protect the brain and spine). Symptoms of sepsis and meningitis may include poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes), grunting breaths and abnormal movements. Cronobacter infection may also cause bowel damage and may spread through the blood to other parts of the body.

It is important to note that this recall is not related to ByHeart’s own manufacturing in any way. In addition, the company has not received any consumer complaints that would indicate any illness, to date; illness complaints are an early detection of safety concerns. If a baby has already consumed all of the formula, there is no reason for concern, and no additional action is needed. If parents have any questions, they should consult with their pediatrician.

ByHeart owns its entire manufacturing supply chain with the exception of final canning, which is conducted by a reputable third-party packager. ByHeart is taking this precautionary measure because one test sample collected from the third-party packaging facility tested positive for Cronobacter sakazakii. All product packaged that day, and the first production on the next day, was isolated for destruction and not distributed. Out of an abundance of caution, we are now recalling all product produced during the entire production run.



As a company committed to parents, ByHeart holds itself to the highest standards when it comes to safety and applauds the FDA’s efforts to oversee the safe manufacturing of infant formula. Parents can remain confident in the safety of ByHeart’s products as the company continues to expand its investments in infant formula innovation, clinical studies, and industry-leading quality standards. ByHeart’s manufacturing facility in Reading, PA, continues to operate 24/7, and the company is committed to providing customers formula in January.

What ByHeart Customers Should Do

Customers who purchased ByHeart product should check the bottom of the can and dispose of product from batches 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1. ByHeart is setting up a webpage at https://byheart.com/notices with additional information about its measures. Should customers have any other questions or want to find out if the product they have is included in the voluntary recall, please email notices@byheart.com or text ByHeart at 1-909-506-2354. The company will also be reaching out directly to all customers via email who purchased orders from these identified batches.

Consumers who purchased Texas oysters since Nov. 17 should check the packaging to see if they were harvested in TX 1. If the oysters were unpackaged, they should contact the seller to find the source. Restaurants should contact their distributor for information on the source of their oysters. Any oysters from TX 1 should be discarded.

DSHS closed the TX 1 area to harvesting on Dec. 8 after receiving reports from health departments in Southeast Texas and Florida that people who had consumed oysters from the area had gotten sick. Reported symptoms include fever, nausea, diarrhea, vomiting, abdominal cramps, chills and headache. People experiencing any of these symptoms after eating oysters should contact their health care provider and tell them about the exposure to oysters. No hospitalizations have been reported at this time.



DSHS epidemiologists are working with local health departments to investigate cases of illness, and DSHS will test water samples collected in the recall area to determine when it may safely reopen to oyster harvesting. No other species of seafood is affected.

The recalled Mint Meltaways were distributed to retail stores in Oregon and Washington and sold nationwide through mail orders since September 21, 2022 to date.

The affected product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC.  The front label is read “Mint Meltaways” and the back label is read “Heirloom Mint Meltaways”. The affected product is marked with lot #032123 on the bottom.



No illnesses or deaths have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the Peanut Butter Meltaways product was mis-labeled as Heirloom Mint Meltaways and peanut was not declared on finished product label.  The firm’s subsequent investigation indicates the problem was caused by a temporary breakdown in the company's packaging process.  The process has been corrected and the company has instituted additional safety checks and corrective actions.

This recall is being made with the knowledge of the U.S. Food and Drug Administration and the Oregon Department of Agriculture.



Consumers with a peanut allergy who have purchased the affected “Mint Meltaways” are urged not to consume the product and dispose of it or return it to their place of purchase for a full refund. Consumers with questions may contact the company at 1-800-527-5748 between 9am and 5:30pm PST, Monday-Friday.

This voluntary recall was issued because some items may be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis.

Units affected by this recall:

Were available for sale at Lidl stores between October 12, 2022 and December 5, 2022

Will have a BEST IF USED BY year of 2023

Will have a barcode number of 4056489516965

This issue was found during routine testing, which Lidl performs on an ongoing basis to help ensure safe and quality products for our customers. Lidl US has received no reports or complaints of illness related to this product to date.

Lidl US takes the health and safety of its customers as its top priority. If customers have purchased this product, they should not consume the product, and immediately return it to their nearest Lidl store for a full refund.

Customers who have questions about this voluntary recall should call the Lidl US Customer Care Hotline at 1-844-747-5435 (8 am-8 pm ET, Monday-Saturday).

Lidl US regrets any inconvenience related to this voluntary recall, which is issued in keeping with our focus on customer health and safety. Our Quality Assurance Department works around-the-clock to ensure that all products on our shelves meet the high-quality standards that we would expect when feeding our own families. We are grateful for all our Lidl US customers who choose to shop with us every day.

FREQUENTLY ASKED QUESTIONS (FAQS):

Q. What products are affected by this recall?

A. This voluntary recall only affects the 8.4 oz Favorina branded Advent Calendar (Premium Chocolate with a Creamy Filling) sold at Lidl US stores between October 12th and December 5th, 2022.

Q. What are the potential issues with the products?

A. This product is being voluntarily recalled due to a potential Salmonella contamination. Salmonella is an organism that poses a serious health risk to young children, pregnant women, the elderly, and others with weakened immune systems.

Q. How is Lidl conducting this recall? How do I participate?

A. We have removed the affected products from our shelves and we are asking all customers who have purchased this product to not consume it and return it to one of our stores for a full refund. Any customers with questions or concerns can contact Lidl Customer Care at (844)-747-5435 (8am-8pm ET, Monday-Saturday).

Q. I no longer have the receipt for the product. Can I still return it?

A. Yes. You can still return the product without a receipt for a full refund.

The fully cooked summer sausage products were produced on July 13, 2022. The following products subject to the public health alert are [view labels]:       

• 1-lb. chubs containing “JET HIGH PRAIRIE MEATS SUMMER SAUSAGE” with lot code 220715 represented on the label.
• 1-lb. chubs containing “FANTASMA’S finest SUMMER SAUSAGE” with lot code 220715 represented on the label.

The products bear establishment number “EST. 31865” inside the USDA mark of inspection. These items were shipped to retail locations in Kansas and Missouri and additional locations through online sales.

The problem was discovered when the firm notified FSIS that they received a customer complaint reporting clear plastic embedded within multiple packages of summer sausage products.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Media and consumers with questions regarding the recall can contact Louis Fantasma, Paradise Locker Meats Plant Manager, at 816-945-9278 or louis@paradisemeats.com.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

The Southern Nevada Health District notified the FDA of two clusters of illnesses from individuals that consumed raw oysters at a restaurant in Las Vegas on 10/28/2022 and 11/5/2022. To date, the Southern Nevada Health District reports one confirmed and nine potential sapovirus illnesses.

Sapoviruses cause a sporadic gastroenteritis, similar to norovirus, in populations ranging from children to the elderly. The infections are more frequent in children under age 5 than in adults. The most common symptoms of sapovirus are diarrhea, vomiting, nausea, and stomach pain. Other symptoms include fever, headache, and body ache. Most people infected with sapovirus begin to develop symptoms 12 to 48 hours after infection. Symptoms usually last one to four days. See more information here.

The recalled Enoki Mushroom was distributed nationwide to distributors and retail stores.



The Enoki Mushroom comes in a 200g/7.05oz clear plastic package with the following description “Enoki Mushroom” in the front and Green Day Produce, Inc. in the back. The UPC is 16430-69080 is located on the back side of the package. There is no lot code or dates on the package.

No illnesses have been reported to date in connection with this problem. The distribution of the product has been suspended.



The potential for contamination was discovered after a retail sample was collected and analyzed by Michigan Department of Agriculture and Rural Development (MDARD) and revealed the presence of Listeria monocytogenes in 200g/7.05 oz. package of Enoki mushroom.



This recall is being made with the knowledge of the U.S. Food and Drug Administration and CDPH.

While no illnesses or injuries have been reported, we took action out of an abundance of caution after a small number of consumers contacted Nestlé USA about this issue.



 

Consumers who may have purchased these three batch codes (22135554RR, 22145554RR, 22155554RR) of Edible Chocolate Chip Cookie Dough tubs from NESTLÉ® TOLL HOUSE® should not consume the product and should return the product to the retailer where it was purchased for a replacement or refund. For any further support needed, please contact Nestlé USA at (800) 681-1678 Monday-Friday from 9 a.m.-6 p.m. EST.