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 

FDA LINK 

FDA LINK 

Western United Fish Company dba Annasea Foods Group of Kent, WA is recalling 3,314.7 lbs. of Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco Item Number of 17193, with the Sell By Date of 9/22/2025, because the green onions used in the product have 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 lead to serious pregnancy complications among pregnant women.

The affected Ahi Tuna Wasabi Poke product is packaged in clear plastic clamshell containers and has the Kirkland Signature brand label with the Pack Date of 9/18/2025 and Sell By Date of 9/22/2025.

Product was sold at the deli section from Costco Warehouse stores in the following states on 9/18/2025: Alabama, Alaska, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Indiana, Louisiana, Maine, Maryland, Massachusetts, Minnesota, Mississippi, Missouri, Montana, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, and Wisconsin.

No illnesses have been reported to date.

This recall was initiated after being notified by our green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke on 9/17/2025. We are continuing to work with our green onion supplier to determine the root cause.

Consumers should not consume this affected product and dispose of it immediately and visit your local Costco for a full refund.

Please call Western United Fresh Co. DBA Annasea Foods Group at (425) 558-7809, 7:00am – 3:30pm Pacific Time, Monday – Friday, or email info@annasea.com if you have any issues or concerns.

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

FDA LINK 

AquaStar (USA) Corp of Seattle, WA is recalling:

approximately 49,920 bags (net wt. 2lbs) of Kroger Raw Colossal EZ Peel Shrimp.
approximately 18,000 bags (net wt. 2lbs) of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp.
approximately 17,264 bags (net wt. 1.25lbs) of AquaStar Raw Peeled Tail-on Shrimp Skewers because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with cesium-137 (Cs-137).

Cs-137 is a man-made radioisotope of cesium. Traces of Cs-137 are widespread and can be present in the environment at background levels, and at higher levels in water or foods grown, raised, or produced in areas with environmental contamination. The primary health effect of concern following longer term, repeated low dose exposure (e.g., through consumption of contaminated food or water over time) is an elevated risk of cancer, resulting from damage to DNA within living cells of the body.

The affected shrimp was sold at Baker’s, City Market, Dillons, Food 4 Less, Foodsco, Fred Meyer, Fry’s, Gerbes, Jay C, King Soopers, Kroger, Mariano’s, Metro Market, Pay Less Supermarkets, Pick ‘n Save, Ralphs, Smith’s and QFC in AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NE, NM, NV, OH, OR, SC, TN, TX, UT, VA, WA, WI, WV and WY between June 12, 2025 and September 17, 2025.

The recalled Kroger Raw Colossal EZ Peel Shrimp net wt. 2lbs., is packaged in transparent printed bag with a blue band on the top with yellow and red details, and has the following codes:

• UPC 20011110643906, lot code 10662 5085 10, Best If Used By: 03 26 27
• UPC 20011110643906, lot code 10662 5097 11, Best If Used By: 04 07 27
• UPC 20011110643906, lot code 10662 5106 11, Best If Used By: 04 16 27
• UPC 20011110643906, lot code 10662 5107 10, Best If Used By: 04 17 27
• UPC 20011110643906, lot code 10662 5111 11, Best If Used By: 04 21 27
• UPC 20011110643906, lot code 10662 5112 10, Best If Used By: 04 22 27
• UPC 20011110643906, lot code 10662 5113 10, Best If Used By: 04 23 27
• UPC 20011110643906, lot code 10662 5113 11, Best If Used By: 04 23 27
• UPC 20011110643906, lot code 10662 5114 10, Best If Used By: 04 24 27
• UPC 20011110643906, lot code 10662 5114 11, Best If Used By: 04 24 27

The recalled Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt. 2lbs., is packaged in clear plastic bag and has a white label with green stripes on top of each bag and has the following codes:

• UPC 011110626196, lot code 10662 5112 11, Best Before: 10 22 2027
• UPC 011110626196, lot code 10662 5113 10, Best Before: 10 23 2027

The recalled AquaStar Raw Peeled Tail-on Shrimp Skewers; net wt. 1.25 lbs., is packaged in a printed bag with a black top and blue bottom and printed pictures of the skewers inside, and has the following codes:

• UPC 731149390010, lot code 10662 5127 10, Best If Used By: 11 07 2027
• UPC 731149390010, lot code 10662 5128 11, Best If Used By: 11 08 2027
• UPC 731149390010, lot code 10662 5133 11, Best If Used By: 11 13 2027
• UPC 731149390010, lot code 10662 5135 10, Best If Used By: 11 15 2027

The FDA is actively investigating reports of Cesium-137 (Cs-137) contamination in shipping containers and frozen shrimp products processed by PT. Bahari Makmur Sejati (doing business as BMS Foods) of Indonesia. No illnesses have been reported to date. As noted in the FDA statement issued on 8/19/25: “At this time, no product that has tested positive or alerted for Cesium-137 (Cs-137) has entered the U.S. commerce.”

“FDA is working with distributors and retailers that received product from PT. Bahari Makmur Sejati after the date of first detection of Cs-137 by Customs & Border Protection (CBP), but from shipments that did not alert for Cs-137, to recommend that firms conduct a recall. In conjunction with other information, FDA determined that product from PT. Bahari Makmur Sejati violates the Federal Food, Drug, & Cosmetic Act in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with Cs-137 and may pose a safety concern.”

Consumers who have purchased affected shrimps should not consume the product and should dispose of or return it to the place of purchase for a full refund.

Consumers with questions may contact the company at 1-800-331-3440, Monday-Friday, 8am-5 pm PST.

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

FDA LINK

Lawrence Wholesale LLC of Vernon, CA is recalling a limited quantity of Kroger bagged frozen shrimp and Kroger frozen shrimp products because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with Cesium-137 (Cs-137).

Cs-137 is a man-made radioisotope of cesium. Traces of Cs-137 are widespread and can be present in the environment at background levels, and at higher levels in water or foods grown, raised, or produced in areas with environmental contamination. The primary health effect of concern following longer term, repeated low dose exposure (e.g., through consumption of contaminated food or water over time) is an elevated risk of cancer, resulting from damage to DNA within living cells of the body.

Bagged frozen shrimp and shrimp cocktail products were sold by Kroger in the following states: AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NE, NM, NV, OH, OR, SC, TN, TX, UT, VA, WA, WI, WV and WY. The product has the following descriptions and codes:

The FDA is actively investigating reports of Cs-137 contamination in shipping containers and frozen shrimp products manufactured in Indonesia by PT. Bahari Makmur Sejati (doing business as BMS Foods). No illnesses have been reported to date. As noted in the FDA statement issued on 8/19/25: “At this time, no product that has tested positive or alerted for Cesium-137 (Cs-137) has entered the U.S. commerce.”

FDA is working with distributors and retailers that received product from PT. Bahari Makmur Sejati after the date of first detection of Cs-137 by Customs & Border Protection (CBP), but from shipments that did not alert for Cs-137, to recommend that firms conduct a recall. In conjunction with other information, FDA determined that product from PT. Bahari Makmur Sejati violates the Federal Food, Drug, & Cosmetic Act in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with Cs-137 and may pose a safety concern.

Consumers who have purchased the recalled bagged frozen shrimp or frozen shrimp products should not consume the product and should dispose of the product or return it to the place of purchase for a full refund. Consumers with questions may contact the company at (323) 235-7535, Monday to Friday from 9:00 am to 4:00 pm PT.

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

FDA LINK

Sprout Organics has initiated a voluntary recall of one lot of Sprout Organics® Sweet Potato Apple and Spinach because it may contain elevated levels of lead.

Exposure to lead, even at low levels, may increase blood lead levels. Additional signs and symptoms of lead exposure are more likely with acute exposure to higher levels of lead or chronic exposure to lead. The effects of lead depend upon the amount and duration of exposure and age/body weight. If a child is exposed to enough lead for a protracted period of time, this can affect learning and development or cause other long-term health problems.

The product, a 3.5-ounce pouch, was sold in Walgreens and some independent stores in the US South region with most sales occurring between September and December 2024. The product was not sold in any other large grocery chain besides Walgreens.

If consumers have product matching the following description in their possession, they should return it to their local store for a full refund. The lot code and expiration date are printed on the bottom strip on the back of the pouch (see photos attached).

No illnesses have been reported to date and no other Sprout Organics products are impacted by this voluntary recall. The voluntary recall is being initiated after routine sampling.

To learn about Sprout Organics comprehensive testing program of ingredients and products before distribution, please go to https://sproutorganics.com/pages/faqExternal Link Disclaimer.

Consumers with questions should contact the company at 510-833-6089 Monday through Friday 9 am to 5 pm Pacific Time or by email at Info@sproutorganics.com.