FDA LINK

Danone U.S. is voluntarily recalling its So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints with multiple best-by expiration dates before 08 Aug 2027 at retail stores nationwide due to the potential presence of foreign materials, such as small stones and other hard objects, within the cashew inclusions.

This issue and recall is only isolated to the Salted Caramel Cluster Non-Dairy Frozen Dessert pint item with the indicated best-by dates and codes, as summarized in the table below. No other So Delicious Dairy Free® codes, flavors, or products are impacted.

This voluntary recall was initiated on December 15, 2025. The FDA has been informed of this voluntary recall and So Delicious Dairy Free® is working swiftly with retail partners to remove the potentially impacted product from shelves. In the meantime, the company has already identified and corrected this issue and will soon be able to bring back the frozen dessert so many people enjoy.

So Delicious Dairy Free® takes every consumer experience seriously and is initiating this voluntary recall in line with its commitment to product quality and consumer safety.

Consumers who have purchased the affected product should not consume it. For information on refunds, please contact the So Delicious Dairy Free® Care Line at 1-833-367-8975. Consumer Care specialists are available to speak live during business hours (Monday – Friday; 9am – 6pm EST). Consumers may also reach out to the Consumer Care team via webform at https://sodeliciousdairyfree.com/contact-us/External Link Disclaimer.

Packages / containers will appear as below. Packaging graphics for this product changed in February 2025 (no change to UPC).

FDA LINK

Prime Food Processing LLC of Brooklyn, NY is voluntarily recalling 2,243 cases of two dessert bun varieties because the packaging does not declare milk in the “Contains” allergen statement as required by the U.S. Food and Drug Administration (FDA). The milk in these products is derived from unsalted butter listed in the ingredient statement. People who have an allergy or severe sensitivity to milk risk a serious or life-threatening allergic reaction if they consume these products.

The recalled products were distributed to Asian grocery stores between April 2, 2025 and November 14, 2025 in the following states:

AL, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, RI, TN, TX, UT, VA, WA, WI

Recalled Products include:

Prime Food brand Lava Bun with Salted Egg Yolk with UPC #97903705873- 24 oz Item #PD4188 – This product is packaged in an orange pouch approximately 10.25″W × 11.25″H Lot Code Range: 25092-25318. Expiration Range: 07/26-03/27

Prime Food brand Lava Bun with Green Tea Flavor UPC #97803705883- 24 oz Item #PD4198 – This product is packaged in a bright lime green pouch approximately 10.25″W × 11.25″H Lot Code Range: 25092-25318. Expiration Range: 07/26-03/27

No illnesses or allergic reactions have been reported to date.

The issue was identified during an internal product review. The recall was initiated after it was discovered that packaging did not declare milk in the allergen statement. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company’s label review process.

Consumers who purchased these products should return them to the place of purchase with the uneaten buns and packaging for a full refund.

Consumers with questions may contact Prime Food Processing LLC at 718-963-2323, Monday–Friday, 9:00 AM to 5:00 PM EST.

FDA LINK

The Ambriola Company is recalling select cheese products after routine testing confirmed the presence of 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. Out of an abundance of caution, the Company is also recalling additional cheese products processed at the same facility in West Caldwell, New Jersey.

No illnesses have been reported to date. That said, customers who have symptoms of listeria infection should contact their healthcare provider.

The affected products were distributed to retail stores and distributors nationwide between November 3, 2025 and November 20, 2025 and include:

No other Ambriola, Locatelli, Member’s Mark, Pinna, or Boar’s Head products are included in the recall.

Customers who purchased the affected products should not consume them and either dispose of them or return them to the place of purchase for a full refund. For more information, contact Ambriola at 1-800-962-8224 from Monday through Friday from 9:00am – 4:00 pm ET.

“We take food safety very seriously and immediately alerted stores and distributors to remove the affected products from shelves,” said Phil Marfuggi, chief executive officer. “We are working closely with the FDA and continuing to test our products and facilities to fully understand the situation.”

Ambriola has suspended production and distribution of affected products as the Company conducts a thorough review of all sanitation and food safety procedures.

FDA LINK

Mondelēz Global LLC announced today a voluntary recall of 70 cases of RITZ Peanut Butter Cracker Sandwiches and sold in the following U.S. states: New York, New Jersey, Pennsylvania, Georgia, Arkansas, Missouri, Oklahoma, and Alabama.

This recall is limited to 1 SKU and 2 Code Dates previously recalled in July. This action is not an expansion of that prior recall and is being conducted out of an abundance of caution.

The affected cartons include individually wrapped packs that may be incorrectly labeled as Cheese variety even though the product may be a Peanut Butter variety. People who have an allergy or severe sensitivity to peanuts may risk serious or life-threatening allergic reactions by consuming this product.

All outer cartons affected are labeled correctly and provide an allergen advisory statement indicating that the product “contains peanuts.”

This recall is exclusively for the RITZ Peanut Butter Cracker Sandwich cartons with Best When Used By Dates listed in the grid below, available at a limited number of retail stores nationwide. No other RITZ products or Mondelēz Global LLC products are included in, or affected by, this recall.

Cartons containing only RITZ Cheese Cracker Sandwiches are not affected. In addition, cartons containing either RITZ Peanut Butter Cracker Sandwiches or RITZ Filled Cracker Sandwich Variety Pack with different Best When Used By Dates and Plant Codes than those listed in the above grid are not affected by this recall.

There have been no reports of injury or illness reported to Mondelēz Global LLC to date related to this product, and we are issuing this recall out of an abundance of caution.

The recall was initiated after Mondelēz Global LLC discovered that 70 cases were inadvertently shipped to a limited number of retailers in eight states. Corrective actions are being taken.

Consumers who have a peanut allergy should not eat these products and should discard any product identified in the grid above. Consumers can contact the company at 1-844-366-1171 Monday–Friday, 9 am to 6 pm ET.

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

About Mondelēz International
Mondelēz International, Inc. (Nasdaq: MDLZExternal Link Disclaimer) empowers people to snack right in over 150 countries around the world. With 2024 net revenues of approximately $36.4 billion, MDLZ is leading the future of snacking with iconic global and local brands such as OREO, RITZ, LU, CLIF BAR and TATE’S BAKE SHOP biscuits and baked snacks, as well as CADBURY DAIRY MILK, MILKA and TOBLERONE chocolate. Mondelēz International is a proud member of the Standard and Poor’s 500, Nasdaq 100 and Dow Jones Sustainability Index. Visit www.mondelezinternational.comExternal Link Disclaimer or follow the company on X at www.x.com/MDLZExternal Link Disclaimer.

Contacts:
Jane Corcoran 847-943-5678
news@mdlz.comExternal Link Disclaimer

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/4e189f10-e777-4093ab13-2d517ca70cd1External Link Disclaimer

FDA Link

Silvestri Sweets Inc. of Geneva, IL is voluntarily recalling its 5-ounce bags of Choceur branded Holiday Barks because they may contain undeclared allergens.

Choceur branded Cookie Butter Holiday Bark may contain undeclared pecans. People who have allergies to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.

Choceur branded Pecan, Cranberry & Cinnamon Holiday Bark may contain undeclared wheat. People who have allergies to wheat run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled items were distributed nationwide through Aldi grocery stores.

Cookie Butter Holiday Bark is packed in 5 oz. Choceur branded stand up pouch bags with the lot # 29225 and best by date on 05/2026, which are printed on the back of each bag.

Pecan, Cranberry & Cinnamon Holiday Bark is packed in 5 oz. Choceur branded stand up pouch bags with the lot # 29225 and best by date on 08/2026, which are printed on the back of each bag.

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

The recall was initiated after it was discovered that the Pecan, Cranberry & Cinnamon Holiday Bark had been packaged in Cookie Butter Holiday Bark packages resulting in undeclared pecan, and that the Cookie Butter Holiday Bark has been packaged in Pecan, Cranberry & Cinnamon Holiday Bark packages resulting in undeclared wheat. Subsequent investigation indicates the problem may have been caused by a temporary breakdown in the company’s production and packaging process.

Consumers who have purchased the recalled products are urged to discard the product.

Consumers with questions may contact Silvestri Sweets at 1-630-232-2500 – M-F 8:30am – 4:30pm CST.

UPDATE:

ByHeart a next-generation baby nutrition company, announced today that it is expanding its voluntary recall to include all batches of ByHeart Whole Nutrition Infant Formula cans and Anywhere Pack™ nationwide. This action is being taken in close collaboration with the U.S. Food and Drug Administration (FDA), despite the fact that no unopened ByHeart product has tested positive for Clostridium botulinum spores or toxin. This action underscores ByHeart’s core mission: protecting babies above all else.

“The safety and well-being of every infant who uses our formula is, and always will be, our highest priority,” said Mia Funt, Co-Founder and President of ByHeart. “This nationwide recall reflects our commitment to protecting babies and giving families clear, actionable information. Alongside this recall, we are conducting a comprehensive investigation to do our part to get the answers parents expect and deserve.

While the FDA is awaiting confirmed results of its testing, ByHeart is taking proactive steps to do all it can to protect families. The company is actively:

• Recalling all product from the market while the FDA’s comprehensive investigation seeks to identify a root cause of the broader outbreak
• Testing every batch of formula with an independent third-party laboratory—a process which has already begun
• Providing FDA and the California Department of Public Health (CDPH) full access to our facilities and unopened cans to conduct testing without restriction
• Sharing results from both regulatory and independent testing publicly as they become available

Infant botulism is a rare but serious illness that occurs when Clostridium botulinum spores are ingested and then colonize the intestinal tract, producing botulinum neurotoxins in the immature gut of infants. Affected infants can present with some or all of the following signs and symptoms: constipation, poor feeding, ptosis (drooping eyelid), sluggish pupils, low muscle tone, difficulty sucking and swallowing, weak or altered cry, generalized weakness, respiratory difficulty, and possible respiratory arrest. If your child is experiencing any of these symptoms, please seek medical attention immediately.

The FDA and CDC have been conducting a broader investigation into a spike of 84 infant botulism cases that started in August. Once ByHeart was alerted on November 7, 2025, the company acted decisively. The results of the FDA’s investigation into the broader cases will help inform any additional steps as our own investigation continues.

What Consumers Should Do:

Consumers who have purchased ByHeart Whole Nutrition Infant Formula cans and Anywhere Pack™ should immediately discontinue use and dispose of the product.

If your infant is experiencing symptoms related to infant botulism, contact your health care provider immediately. To report an illness or adverse event, you can:

• Call an FDA Consumer Complaint Coordinator if you wish to speak directly to a person about your problem.
• Complete an electronic Voluntary MedWatch form online.
• Complete a paper Voluntary MedWatch form that can be mailed to the FDA.

If any parents have questions please contact our experts at hello@byheart.com. For more information visit byheart.com External Link Disclaimeror call 1 (833) 429-4327 We are available 24/7.

Media Contact:

ByHeart Public Relations – press@byheart.com

Product Details for Voluntary Recall:

The voluntary recall now applies to all batches of ByHeart Whole Nutrition Infant Formula cans and all Anywhere Packs:

• Can UPC: 85004496800
• Anywhere Pack (™) UPC: 85004496802
• Product Image:

Link to Original Recall

FDA Outbreak Advisory

FDA LINK

 ByHeartExternal Link Disclaimer, a next-generation baby nutrition company, announced today that, out of an abundance of caution, it has chosen to voluntarily recall two batches of ByHeart Whole Nutrition Infant Formula following notification from the U.S. Food and Drug Administration (FDA) of a broader ongoing investigation into a recent outbreak of infant botulism.

Infant botulism is a rare but potentially fatal illness that presents a serious threat to the health of infants which occurs when Clostridium botulinum spores are ingested and colonize the intestinal tract, producing botulinum neurotoxins in the immature gut of infants. Affected infants can present with some or all of the following signs and symptoms: constipation, poor feeding, ptosis (drooping eyelid), sluggish pupils, low muscle tone, difficulty sucking and swallowing, weak or altered cry, generalized weakness, respiratory difficulty, and possibly respiratory arrest.

• The FDA has an ongoing investigation of infant botulism among babies in the U.S.
• The FDA has not identified a direct link between any infant formula and these cases and there is no historical precedent of infant formula causing infant botulism.
• ByHeart is taking the proactive step to remove any potential risk from the market and ensure the highest level of safety for infants.

ByHeart was notified by the FDA on November 7, 2025 of an estimated 83 cases of infant botulism that were reported nationwide since August 2025. Of these, the FDA also noted that 13 infants received ByHeart formula at some point. The FDA has not identified a direct link between any infant formula and these cases and there is no historical precedent of infant formula causing infant botulism. Botulism is extremely uncommon in dairy products or infant formula, and is naturally occurring in environmental sources like soil, select vegetables, and dust.

ByHeart adheres to the highest standards of Global and U.S. recommendations for product testing and safety. No ByHeart product has tested positive for any contaminants.

“The safety and well-being of every infant who uses our formula is our absolute highest priority,” said Mia Funt, Co-Founder and President. “We take any potential safety concern extremely seriously, and act quickly to protect families. As parents ourselves, we understand the concern this news may raise. This voluntary recall is out of an abundance of caution and comes from our ongoing commitment to transparency and safety for babies and their parents. While no testing by ByHeart or regulatory agencies has confirmed the presence of Clostridium botulinum spores or toxin in any ByHeart product, we are taking this proactive step to remove any potential risk from the market and ensure the highest level of safety for infants.”

Product Details for Voluntary Recall:

The voluntary recall applies to the following two batches of ByHeart infant formula:

• Batch Code: 251261P2, Use by: 01 Dec 2026
• Batch Code: 251131P2, Use by: 01 Dec 2026
• UPC: 5004496800
• Product Image : See below

The batch code and use by can be found on the bottom of the can.

No other ByHeart batches are impacted by this voluntary recall.

What Consumers Should Do:

Consumers who have purchased ByHeart infant formula from the identified batch codes should immediately discontinue use and dispose of the product. If you’ve discarded any formula from the following batches, ByHeart will replace those cans at no cost.

If your infant is experiencing symptoms related to infant botulism, contact your health care provider immediately. To report an illness or adverse event, you can:

• Call an FDA Consumer Complaint Coordinator if you wish to speak directly to a person about your problem.
• Complete an electronic Voluntary MedWatch form online.
• Complete a paper Voluntary MedWatch form that can be mailed to the FDA.

If any parents have questions please contact our experts at hello@byheart.com. For more information visit byheart.comExternal Link Disclaimer or call 1 (833) 429 – 4327 We are available 24/7.

FDA Outbreak Advisory

FDA LINK 

Dreyer’s Grand Ice Cream, Inc. is voluntarily recalling a limited number of its Häagen-Dazs Chocolate Dark Chocolate Mini Bars that may contain undeclared wheat. Those with an allergy or severe sensitivity to wheat run the risk of serious or life-threatening allergic reaction if they consume these products.

The affected product is Häagen-Dazs Chocolate Dark Chocolate Mini Bars in the 6-count package with batch code LLA519501 and a Best By date of January 31, 2027.

The affected product was shipped to two retail customers, Kroger and Giant Eagle, in the following states:

• Kroger: (AL, AK, AZ, AR, CA, CO, GA, ID, IL, IN, KS, KY, MI, MS, MO, MT, NE, NV, NM, OH, OR, SC, TN, UT, VA, WA, WV, WI, WY)
• Giant Eagle: (IN, MD, OH, PA, WV)

Batch codes can be identified on the product packaging. Please use the reference images below and look for the batch code LLA519501 under “Best By 31 JAN 2027.”

No other Häagen-Dazs products or other batches of Häagen-Dazs Chocolate Dark Chocolate Mini Bars are affected by this recall.

No illnesses or injuries have been reported to date. We are recalling this product because it may contain products that contain wheat in packaging that does not reveal the presence of wheat on the label. Although our investigation is ongoing, we believe products containing wheat were repacked into the incorrect packaging at the beginning of a production run.

Consumers with a wheat allergy or sensitivity who have purchased the affected product are urged not to consume the product and instead dispose of it or return it to their place of purchase for a full refund.

The safety, quality, and integrity of our products remain our number one priority. We sincerely apologize for any inconvenience this action represents to both our consumers and retail customers.

We are working with the U.S. Food and Drug Administration (FDA) on this voluntary recall and will cooperate with them fully.

Consumers with questions may contact Dreyer’s Grand Ice Cream, Inc. at dreyers@casupport.com.

Dreyer’s Grand Ice Cream, Inc Media Contacts:

Customer Service Phone: 800-767-0120 Monday thru Friday 8am to 5pm EST

FDA LINK

Moonlight Companies is voluntarily recalling California-grown conventional yellow and white peaches because they have the potential to be contaminated with Listeria monocytogenes, an organism that 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 peaches were sold at retail stores nationwide between September 16, 2025 and October 29, 2025. The peaches were either sold as individual pieces of fruit bearing PLU stickers or as multi-packs. This recall does not include packages or PLU stickers with the words “Washington” and/or “Organic.” The recalled products are listed in the following summary table and images are below.

This recall is being conducted because Listeria monocytogenes was identified in the packing facility environment.

No illnesses have been reported to date.

Consumers with questions can contact 855-215-5017, Monday – Friday from 8 am – 5 pm Eastern Time.

This recall is being carried out with the knowledge of the U.S. Food and Drug Administration.

Tai Foong USA of Seattle, Washington is recalling a limited quantity of Fusia Asian Inspirations Veggie Spring Rolls, net wt. 10oz, because the product may contain shrimp, a known allergen, that is not declared on the label. People who have an allergy or severe sensitivity to shrimp or shellfish run the risk of a serious or life-threatening allergic reaction if they consume this product.

The affected Veggie Spring Rolls were distributed exclusively to ALDI stores nationwide and sold under the Fusia Asian Inspirations brand.

The product is a 10-ounce (283.5 g) retail package identified by UPC 4099100222258 and the Best Before date 05/17/2027 printed on the back panel of the retail box.

No other Fusia Asian Inspirations products are affected by this recall.

The recall was initiated after it was discovered that certain cases of Shrimp Spring Rolls may have been inadvertently packaged in boxes labeled as Vegetable Spring Rolls. The cause of this labeling error is being investigated. The recall is being conducted in cooperation with ALDI and the U.S. Food and Drug Administration.

At this time, no confirmed allergic reactions or illnesses have been reported related to this issue.

Consumers who have purchased this product should not consume it. The product should be discarded or returned to the place of purchase for a full refund.

Consumers with questions may contact Tai Foong USA at (206) 883-2317, Monday through Friday, 8:00 a.m. to 5:00 p.m. Pacific Time, or by email at bcox@northernchef.com

LINK