Dietary Supplement and Drug Recalls
Fresenius Kabi USA, LLC recalls Fresenius Kabi Famotidine Injection, USP 20 mg per 2 mL
Nov. 6,2025 – LAKE ZURICH, Ill.— Fresenius Kabi, part of the global healthcare company Fresenius, and a leading provider of essential medicines and medical technologies is voluntarily recalling three lots (numbers 6133156, 6133194, 6133388) of Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL Fill in a 2 mL vial. This recall is being performed to the user level in the United States.
The product is being recalled due to out-of-specification (OOS) endotoxin results of certain reserve samples from a single lot. Based upon the investigation, two additional lots were also included in the recall as a precautionary measure.
Elevated endotoxin levels can precipitate severe systemic reactions such as sepsis and septic shock. Severe responses may include inflammatory and life-threatening immune responses and death. Non-serious adverse event reports potentially associated with the OOS have been received for one lot. These non-serious adverse events included chills, change in mental status, change in respiratory status, fever, increase in body temperature, shivering and shaking. To date, no adverse event reports have been received for the second and third lots.
SiluetaYa recalls SiluetaYa Tejocote Root dietary supplement
SiluetaYa Recalls Tejocote Product Because of Possible Health Risk
SiluetaYa is recalling its tejocote root because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides, which are highly toxic to humans and animals. Ingestion of yellow oleander can cause severe or even fatal neurological, gastrointestinal, and cardiovascular adverse health effects. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, changes in heart rhythm, arrhythmia, and more.
The tejocote root was distributed online.
The product comes in an 8-ounce container.
No illnesses have been reported to date.
The recall was the result of sampling conducted by the FDA.
Food and Beverage Recalls
Africa Imports recalls Africa Imports Organic Moringa Leaf Powder
Africa Imports is voluntarily recalling its Organic Moringa Leaf Powder (1 kilogram box) because it may be contaminated with Salmonella, an organism that can cause serious and sometimes fatal infections in young children, the elderly, and individuals with weakened immune systems. Healthy persons infected with Salmonella may experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare cases, infection can lead to more severe conditions such as arterial infections, endocarditis, or arthritis.
The recalled Organic Moringa Leaf Powder was sold nationwide through the company’s website, africaimports.com. The affected product is packaged in 1-kilogram boxes labeled “Organic Moringa Leaf Powder.” Photos of the affected product are attached to this notice to assist customers in identifying the product. All Organic Moringa Leaf Powder purchased after 06/05/2025 is included in this recall.
As of today (November 6, 2025), we have not been informed of any illness from the Moringa powder sold in this lot.
African Food on Wheels Inc. recalls African Food on Wheels Inc. Oven Dried Fish (Scomberomorus cavalla)
African Food on Wheels Inc. of Bronx, NY is recalling 28 boxes of Product, because it is a dried, un-eviscerated (internal organs not removed) fish greater than 5 inches and length and has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
Oven Dried Fish (SCOMBEROMORUS CAVALLA) was distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only.
Products are packed in a corrugated brown box.
No illnesses have been reported to date.
Blue Oven Bakery, Inc recalls Blue Oven Bakery, Inc English muffin
Cincinnati, Ohio (October 31, 2025) Blue Oven Bakery, Inc. is issuing a voluntary recall on their english muffin for misbranding due to the milk allergen not being declared on the label. The english muffin was sold fresh as a baked product in a 13.04 oz sealed plastic bag.
These products have been produced since 04/24/25 with the last production date of 10/24/2025, and were sold at the following locations:
- Harvest Market- 308 Main St. Milford, OH 45150
- Country Fresh Market- 8315 Beechmont Ave. #15 Cincinnati, OH 45255
- Kremers Market- 755 Buttermilk Pike Crescent Springs, KY 41017
- Back Ally Mercantile- 221 Walnut St. #102 Lawrenceburg, IN 47025
- European Cafe- 9450 Montgomery Rd. Cincinnati, OH 45242
ByHeart Inc. recalls ByHeart Whole Nutrition Infant formula
[New York, NY] – ByHeart, 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 Inc. recalls ByHeart Whole Nutrition Infant formula 24 oz cans and 0.6oz packets
ByHeart Broadens Voluntary Recall While Investigation Continues
[New York, NY] – 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:
JFE Franchising Inc. recalls Snow Fruit Peach Salsa
Houston, TX (November 3, 2025) - JFE Franchising, Inc. of Houston, TX, is voluntarily recalling a limited number of products containing California-grown yellow and white peaches because they may be contaminated with Listeria
Listeria monocytogenes is commonly known for causing fever, muscle aches, nausea, vomiting, and diarrhea and may also lead to stillbirth in severe cases. People exhibiting any of these symptoms should seek medical attention immediately.
There have been no illnesses or consumer complaints reported to date.
Moonlight Companies recalls Moonlight/Kroger Yellow and white peaches
October 29, 2025 (Updated November 8, 2025) – 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.
Read Comments