FDA LINK

Beekeeper’s Naturals is voluntarily recalling lot # 5950, Exp. Date 02/2028 of Beekeeper’s Naturals Saline Nasal Spray, sold only through Amazon, to the consumer level. This lot, produced at a third-party manufacturer, tested above our acceptable microbiological limits for yeast and may contain Aspergillus spp.

In the population most at risk, such as people with weakened immune systems or lung diseases, there is a reasonable probability that use of the product with Aspergillus spp. contamination will cause serious and life-threatening infections such as invasive sinusitis and lung infections.

To date, Beekeeper’s Naturals has received four reports from customers regarding adverse reactions potentially related to the recalled product, including sinus congestion, irritation or infection.

Beekeeper’s Naturals Saline Nasal Spray is used as a sinus congestion rinse. The product is sold in a single-unit 1 FL OZ. (30 mL) bottle and the lot number (5950) and expiration date (02/2028) can be found on the bottom or back label.

Five hundred and eighty-five (585) units of this lot 5950 were sold through Amazon between April 2 and April 24, 2026. Due to a clerical error, this lot 5950 was mistakenly shipped to Amazon before testing results became available. Working with Amazon, we have already directly notified all purchasers of this lot 5950 of Beekeeper’s Naturals Saline Nasal Spray.

No other Beekeeper’s Naturals products, including Nasal Spray Max, are impacted by this voluntary recall.

If you think you have this lot of Beekeeper’s Naturals Saline Nasal Spray:

• Check the lot number on the bottom or back label of your Beekeeper’s Naturals Saline Nasal Spray
• If it reads Lot 5950 (Best By: 02/2028), discontinue use
• Contact us at contact@beekeepersnaturals.com or 1-888-759-6910, Monday-Friday 8am to 8pm ET, for a refund, or if you have any other questions.
• If you have experienced any problems that may be related to taking or using this product, contact your physician or healthcare provider

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

• Complete and submit the report Online: www.fda.gov/medwatch/report.htm
• Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

Beekeeper’s Naturals has taken immediate corrective action to identify and resolve the source of the concern. We remain fully committed to the rigorous quality standards our customers expect from us.

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

FDA LINK

Nara Organics of New York, NY, is voluntarily recalling all lots of Nara Organics Powdered Infant Formula currently on the market out of an abundance of caution due to the potential risk of Clostridium botulinum contamination.

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.

Nara Organics Powdered Infant Formula was distributed nationally across Target retail stores, Target.com, and Nara.com between July 2025 and June 2026. Nara Infant Formula is not distributed outside of the USA.

Affected Product Details:

• Nara Organics Whole Milk Infant Formula, 700g, with UPC 860013251901
• Nara Organics Whole Milk Infant Formula, 400g, with UPC: 860013251918

All lots currently on the market are included in this voluntary recall, and the specific codes are as follows. The lot code can be found on the bottom of each can.

• 408125075E14F2
• 708125076E14F2
• 708125083E14F2
• 408125139E14F2
• 708125141E14F2
• 708125145E14F2
• 708125174E14F2
• 709125273E14F2
• 709125280E14F2
• 709125288E14F2
• 409125307E14F2
• 70926019ENNB
• 70926029ENNB
• 70926035ENNB
• 70926039ENNB
• 70926042ENNB

The Food and Drug Administration (FDA) and Center for Disease Control (CDC) contacted Nara Organics late Friday, June 12, 2026, and provided information about 3 cases of infant botulism in infants who CDC reported had consumed Nara formula. The 3 infants were hospitalized and treated with BabyBIG (Botulism Immune Globulin Intravenous) in California, Washington, and Pennsylvania. There are no reported deaths. The three specific product lots these infants were exposed to are: 709125280E14F2, 709125288E14F2, 708125174E14F2. To date, Nara infant formula has not tested positive for C. botulinum. However, Nara is voluntarily recalling all products currently in market.

Nara is taking aggressive action to ensure the safety of the babies and families who use the product as we work closely with the FDA, Centers for Disease Control and Prevention (CDC), and state partners to support their investigation into the root causes of these cases.

Customers should stop using the affected products immediately. If your baby has consumed this product and is presenting symptoms of infant botulism including, but not limited to vomiting, diarrhea, constipation, poor feeding, drooping eyelids, and weak crying, please contact your healthcare provider for immediate care.

To report an illness or adverse event, you can:

• Report a Product Problem through SmartHub
• Complete an electronic Voluntary MedWatch form online
• Complete a paper Voluntary MedWatch form that can be mailed to FDA

Nara will automatically refund all consumers who purchased formula from their website in May and June 2026. Other customers with unused product may request a refund by taking a photo of the bottom of each can and completing the refund form here:

https://nara.com/pages/refund-request-formExternal Link Disclaimer. Target customers may return their product to Target retail locations or follow Target’s online return instructions.

We sincerely apologize for the concern and distress this announcement causes our customers. We are committed to leading with transparency and accountability throughout this process as we work to identify further information. We will provide additional information as it becomes available. Customers with questions are encouraged to visit Nara’s website External Link Disclaimeror email hello@nara.com.

FDA Outbreak Advisory

FDA LINK 

Champion Foods LLC of New Boston, Michigan, is voluntarily recalling certain batches of Motor City Pizza Co. 5 Cheese Bread (“5 Cheese Bread”) because they have the potential to be contaminated with Salmonella. This action follows a California Dairies, Inc. milk powder recall due to a concern of potential Salmonella contamination.

Salmonella is an organism that 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 (which may be bloody), 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.

The recalled milk powder was supplied to a third-party manufacturer that provides a seasoning blend used in our 5 cheese sauce blend. To date, neither Champion Foods LLC nor our suppliers have received any reports of illness or injury related to these products. Routine testing conducted by the seasonings blend manufacturer prior to use in the production of the 5 Cheese Bread showed that the seasonings batches tested negative for Salmonella; however, we are taking action out of an abundance of caution for the safety of our customers.

Affected 5 Cheese Bread lots were distributed and sold nationwide at retailers including Costco, Walmart, Giant Landover, Grocery Outlet, Jewel, Kroger, Schnucks, Target, C&S, Bozzuto’s, Brookshire Grocery, Meijer, Food City, KeHe, Lipari, Publix, Merchants Dis Hickory, PDI/Hy-Vee, River Valley, SpartanNash, Supervalu, and UNFI.

The sell by date is printed in black inside the cheese bread image on the front on the pizza.

Consumers who purchased one of the recalled lots listed above may contact Champion Foods LLC directly info@motorcitypizzacompany.com for more information. For media inquiries, please contact media@championfoods.com.

This recall is being conducted in coordination with FDA.

FDA LINK

Target is voluntarily recalling Up & Up Fragrance Free and Up & Up Fresh Cucumber Scented Baby Wipes following customer complaints of product discoloration, and FDA testing that identified the presence of Burkholderia cepacia complex and Burkholderia gladioli in product samples.

Use of products contaminated with Burkholderia cepacia complex and Burkholderia gladioi may result in serious and life-threatening infections. The products are predominantly used on newborns, infants, and young children, who are particularly vulnerable to opportunistic infection due to their immature immune systems. In healthy individuals, use of the product on skin with minor lesions will more likely result in local infections, whereas in immunocompromised individuals, newborns, infants and young children, the infection is more likely to spread into the bloodstream, potentially leading to life-threatening sepsis or pneumonia.

The recalled wipes were manufactured by a supplier, and sold at Target stores nationwide and online at Target.com.

Out of abundance of caution, Target is recalling the following products:

• Up & Up Fragrance Free Baby Wipes
  • 20 Count: UPC 085239265956
  • 72 Count: UPC 085239265949
  • 216 Count: UPC 085239265963
  • 800 Count: UPC 085239266137
  • 1200 Count: UPC 085239266090
• Up & Up Fresh Cucumber Scented Baby Wipes
  • 72 Count: UPC 085239265970
  • 216 Count: UPC 085239265994
  • 800 Count: UPC 085239265987
• The Up & Up Fragrance Free Baby Wipes are packaged in plastic pouches with each pouch containing 20, 72, or 100 wipes. The wipes were sold individually in 20 and 72 count pouches, a bundle of three 72 count pouches (216 wipes) and 100 count pouches packaged in 800 count and 1200 count boxes.
  • Fragrance Free Baby Wipes with a manufacturing date code of November 07, 2025 (071125X/XX) to May 5, 2026 (050526X/XXX) and expiration dates between May 10, 2028 (100528) through November 5, 2028 (051128)
• The Up & Up Fresh Cucumber Scented Baby Wipes are packaged in plastic pouches with each pouch containing 72 or 100 wipes. The wipes were sold individually in 72 count pouches, a bundle of three 72 count pouches (216 wipes) and 100 count pouches packaged in 800 count boxes.
  • Fresh Cucumber Scented Baby Wipes with a manufacturing code of December 29, 2025 (291225X/XX) to December 30, 2025 (301225X/XX) and expiration dates between June 29, 2028 (290628) through June 30, 2028 (300628).

Consumers should immediately stop using the recalled products and return them to any Target store for a full refund. Consumers can contact Target Guest Relations at 1-800-440-0680 from 7 a.m. to 10 p.m. CT daily for more information.

Target and the manufacturer of the wipes, Sapro Temizlik Urunleri, have received a number of consumer complaints and adverse event reports alleging product discoloration and symptoms such as skin irritation, eye irritation, and infections potentially associated with the use of the product. These reports remain under investigation. Target is coordinating with the manufacturer and continues to investigate this matter.

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

FDA LINK

Total Nutrition Inc. of Deer Park, NY is voluntarily expanding its recall of TNVitamins and Doctor’s Pride Ultra Potent Complete Green Superfood Moringa Capsules due to the potential to be contaminated with Salmonella. This expansion follows an ongoing supply chain investigation that identified additional lot numbers linked to the same raw material lot that prompted the original recall. 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 (which may be bloody), 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.

The recalled product was distributed nationally through the online platforms, Amazon, Walmart, TikTok Shop, Target, and the company’s websites, http://www.tnvitamins.com/External Link Disclaimer, and https://www.doctorspride.com/External Link Disclaimer.

The product is packaged in white HDPE supplement bottles with smooth, white caps and 120 clear capsules filled with green moringa powder. Some of the affected lots are:

The recall was initiated following notification from the U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) that these products may be implicated in an ongoing investigation associated with moringa-containing dietary supplement products. Total Nutrition Inc. has ceased distribution and sale of the identified product and has initiated removal orders across all applicable sales and fulfillment channels while the FDA, CDC and the company continue their investigation.

This expansion was discovered during a supply chain traceability review which identified a common raw material from Lot 2507199 or 2512-304, one of the original recalled lots.

Total Nutrition Inc. is including Lots 2503104, and 2725 of TNVitamins Ultra Potent Complete Green Superfood Moringa 10,000 mg and Doctor’s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg in the recall effective immediately.

No other TNVitamins or Doctor’s Pride products are involved.

Customers who have purchased the affected products are asked to dispose of them immediately. Do not eat, sell, or serve the product. Customers may request a refund by contacting TNVitamins at customerservice@tnvitamins.com and providing your name, order number, and a photo of the product with lot codes in question.

We apologize for the inconvenience and concern this recall may cause to our customers. TNVitamins is committed to ensuring the quality of our products and the well-being of our consumers.

FDA LINK

George J. Howe Co. of Grove City, Pennsylvania is voluntarily recalling 13,619 pounds of Sunflower Seeds because it may contain undeclared tree nut (cashew) allergens. Individuals with an allergy or severe sensitivity to tree nuts are at risk of serious or life-threatening allergic reaction if they consume these products. This product is safe to consume for anyone who does not have a Tree Nut (Cashew) allergy or sensitivity to Tree Nuts (Cashews).

The product was distributed in Alabama, Arkansas, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Jersey, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Virginia, Wisconsin and reached consumers through retail grocery chains (including Foodland, Giant Eagle, Piggly Wiggly, Shop Rite, Shop N Save, Walmart and independent grocers), foodservice accounts, specialty retailers, concession/airport operators, and institutional customers across multiple states.

The recalled product can be identified as follows:

• Plastic Stand-Up Pouch Container, 11 oz, Blue with SUNFLOWER SEEDS brand name, “Fresh Roasted Sunflower Seeds, Lightly Salted”, UPC of 073171003163, Best By Expiration Dates of 08/28/2026, 09/18/2026, 10/01/2026, 10/09/2026, 11/18/2026, and 12/12/2026
• Plastic Stand-Up Pouch Container, 11 oz, Blue with SUNFLOWER SEEDS brand name, “Fresh Roasted Sunflower Seeds, No Salt”, UPC of 073171003200, Best By Expiration Dates of 09/24/2026, 10/30/2026, 11/18/2026, and 12/11/2026
• Plastic Tub, 9.5 oz, Gold Label with Sunflower Seeds brand name, “Sunflower Seeds, roasted and salted.”, UPC of 073171027015, Best By Expiration Dates of 7/22/2026 and 09/05/2026

All products declare an allergen warning that “This product was packaged in a facility that also processes peanuts, tree nuts, milk products, soy, wheat and eggs.”

No illnesses have been reported to date.

The voluntary recall was initiated after the company discovered in a routine inspection that Sunflower Seeds containing Tree Nut (Cashews) were distributed in packaging that did not reveal the presence of Tree Nut (Cashews). Subsequent investigation indicates the problem was caused by an oversight in the company’s production process at the changeover of products.

Consumers who have purchased the affected Sunflower Seeds are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the George J Howe Company at (800) 367 4693 M-F 8:00am to 5:00pm EST, or by email at quality@georgehowe.com.

USDA LINK 

FDA LINK

February 13, 2026 – North Kansas City, Missouri, Shaman Botanicals, LLC is voluntarily recalling one lot (Lot B# AAW.501.3) of Alkaloids Chewable Tablets—White Vein to the consumer level. Recent testing showed that the Alkaloids Chewable Tablets—White Vein product contains 7-Hydroxymitragynine (7-OH) in an amount more than the declared value of 7.5 mg/tablet.

Risk Statement: Use of the Alkaloids Chewable Tablets—White Vein product could result in consumers ingesting a higher dose than intended, which could result in adverse health effects.

Shaman Botanicals, LLC has not received any reports of adverse events related to this lot of Alkaloids Chewable Tablets—White Vein.

The product is packaged in a 2-count bag with UPC Code 810057763724, in a 20-count bag with UPC Code 810057763830 and in a 30-count bottle with UPC Code 810057763779. The affected Alkaloids Chewable Tablets—White Vein lot has the following lot number: Lot B# AAW.501.3 (all expiration dates). The product can be identified by the lot number on the package and/or the bottom of the bottle. The Alkaloids Chewable Tablets—White Vein product was distributed nationwide to wholesalers, retailers, and consumers via online sales.

Shaman Botanicals, LLC is notifying its distributors and customers by email and is arranging for return of the affected product and providing refunds or replacement of all recalled products. Wholesalers, distributors, retailers, and consumers that have the Alkaloids Chewable Tablets—White Vein product that is being recalled should quarantine the product, stop using it, and return it to Shaman Botanicals, LLC.

To receive a full refund or replacement product, please go to the attached URL to register your return. https://recall.cbdamericanshaman.com/External Link Disclaimer.

Consumers with questions regarding this recall can contact Shaman Botanicals, LLC, Monday through Friday from 9am-5pm CST, at:

Vince Sanders c/o Quality Department
1501 Iron Street
North Kansas City, MO 64116
Telephone: 855-427-7386
Email: Quality@CBDAmericanShaman.com
https://recall.cbdamericanshaman.com/External Link Disclaimer

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this dietary supplement product.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.

• Complete and submit the report online: www.fda.gov/medwatch/report.htm
• Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form or submit by fax to 1-800-FDA-0178.

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

UPDATE:

Ajinomoto Foods North America, Inc., a Portland, Ore., establishment, is expanding its Feb. 19, 2026, recall of frozen not ready-to-eat (NRTE) chicken products that may be contaminated with foreign material, specifically glass, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The establishment is recalling approximately 33,617,045 additional pounds of various ready-to-eat (RTE) and NRTE chicken and pork fried rice, ramen, and shu mai dumpling products, for a combined total of 36,987,575 pounds subject to recall.

This expansion includes 16 products produced between October 21, 2024, and February 26, 2026, under brand names Ajinomoto, Kroger, Ling Ling, Tai Pei, and Trader Joe’s. These products have best-by dates ranging from February 28, 2026, through August 19, 2027. View product list. View labels.

The products subject to recall bear establishment number P-18356, P-18356B, or P-47971 inside the USDA mark of inspection. The items were shipped to retail locations nationwide. Certain Ajinomoto items were exported to Canada and Mexico.

The problem was discovered when the establishment notified FSIS that it received multiple consumer complaints involving glass found in product. Upon further investigation, the establishment determined that a vegetable source ingredient, specifically carrots, was the likely source of the glass contamination, which also impacted the additional products subject to this expanded recall. There have been no confirmed reports of injury due to consumption of this product. Anyone concerned about an injury should contact a healthcare provider.

FSIS is concerned that some product may be in retailers’ or consumers’ 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.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Members of the media with questions about the recall can contact Corporate PR at MediaInquiry@ajinomotofoods.com or call (909) 477-4800. Consumers with questions about the recall can contact Consumer Affairs, Ajinomoto Foods North America, at (855) 742-5011 or email at customercare@ajinomotofoods.com.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) 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/.

FDA LINK

Ajinomoto Foods North America, Inc., a Portland, Ore. establishment, is recalling approximately 3,370,530 pounds of frozen not ready-to-eat (NRTE) chicken fried rice products that may be contaminated with foreign material, specifically glass, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The NRTE chicken fried rice items were produced between September 8, 2025, and November 17, 2025. The following products are subject to recall [view labels]:

• 1.53-kg. cardboard packages containing 6 bags of frozen “AJINOMOTO YAKITORI CHICKEN WITH JAPANESE-STYLE FRIED RICE” with BEST BEFORE/MEILLEUR AVANT dates 26 SE 09 through 26 NO 12.
• 20-oz. (1 lb. 4 oz.) plastic bag packages containing frozen “TRADER JOE’S Chicken Fried Rice with stir fried rice, vegetables, seasoned dark chicken meat and eggs” with BEST BY dates 9/8/2026 through 11/17/2026.

The products subject to recall bear establishment number P-18356 inside the USDA mark of inspection. The Trader Joe’s item was shipped to Trader Joe’s retail locations nationwide. The Ajinomoto item was exported only to Canada.

The problem was discovered after the establishment notified FSIS that it received four consumer complaints regarding glass found in product. There have been no confirmed reports of injury due to consumption of this product. Anyone concerned about an injury should contact a healthcare provider.

FSIS is concerned that some product may be in retailers’ or consumers’ 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.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Members of the media with questions about the recall can contact Corporate PR at MediaInquiry@ajinomotofoods.com or call (909) 477-4800.  Consumers with questions about the recall can contact Consumer Affairs, Ajinomoto Foods North America, at (855) 742-5011 or email at customercare@ajinomotofoods.com.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) 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/.