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.

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/.

FDA LINK

IF Copack LLC d.b.a. Initiative Foods (“Initiative Foods”) is recalling one lot of the “Tippy Toes” brand Apple Pear Banana Fruit puree (“Product”) due to elevated levels of patulin. Patulin is a naturally occurring substance (called a mycotoxin) which is produced by molds that may grow in various fruits, including apples. Long-term exposure resulting from ingestion of patulin can lead to various adverse health consequences, including a potential for immune suppression, nerve damage, headache, fever, and nausea. No illnesses or injuries have been reported to date.

The Product was distributed nationwide in retail grocery stores in all U.S. states other than Alaska. The Product may have been distributed in the U.S. territories of Guam and Puerto Rico.

Product Information

The “Best By” (expiration) date is found on the bottom of each plastic tub. The recalled Product will have a date stamped as “BB 07/17/2026.” The package is also marked with the package code “INIA0120” as shown below:

The recalled Product was sampled under the Total Diet Study by the U.S. Food and Drug Administration (“FDA”), which found elevated patulin levels higher than is common for these products. Initiative Foods worked with FDA to identify the single lot to recall due to possible health concerns identified in this notice.

This recall is being conducted based on FDA’s recommendation.

Action for Consumer

Consumers with the Product matching the “Best By” (expiration) date of July 17, 2026 should:

• Discontinue use of the Product and dispose of it immediately or return to their place of purchase for a refund.
• Contact their healthcare provider if concerns arise regarding health after consumption of the Product.

Action for Retailers

Retailers should check inventory and shelves, and immediately remove the affected lot from sale or distribution and catalogue the recalled product.

Company Statement

“At Initiative Foods, the safety of our consumers and their families is our highest priority. We are cooperating with the FDA to ensure strict review and enhanced safety measures across all our products. We thank our retail partners and customers for their understanding and prompt action on this matter,” said Don Ephgrave, Initiative Foods’ CEO and President.

More Information

For further recall information and updates, consumers and retailers can call a dedicated toll-free number: 1-855-215-5730, Monday through Friday, 8 a.m. to 5 p.m. Eastern Standard Time.

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

FDA LINK

Ambrosia Brands, LLC of New York, New York is recalling certain lots of its Rosabella Moringa Capsules product due to possible contamination with Salmonella, 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 sold to consumers located nationwide in the United States, through our direct-to-consumer website (tryrosabella.com) and Tik Tok Shop (https://www.tiktok.com/shop/pdp/moringa-capsules-800mg-by-rosabella-for-immune-gut-health-support/1729464033034539782External Link Disclaimer), since February 2025. We are also aware that there may be unauthorized 3rd party distribution to consumers through ebay.com, Shein, or other sites. None of the impacted lots were sold by us on Amazon.com, however, while we do not have any authorized resellers on Amazon.com, we urge you to check your lot numbers for any Rosabella Moringa capsules purchased on the site.

The recall includes the following product and lots:

• Rosabella Moringa Capsules, 60 Count Bottles
• Lots impacted (all start with 1356 as the sku number, and end in a -1 or -2 after the lot code):

The recalled products are packaged in white plastic bottles. The lot code is printed on the bottom of the bottles. The lot code is the middle seven digits of the code printed above the expiration date. Additionally, the affected product has expiration dates from 03/2027 to 11/2027. Please see the example packaging and lot code below.

No other Ambrosia Brands products are impacted by this recall.

To date, there have been 7 illnesses resulting in 3 hospitalizations across the United States due to Salmonella contamination, 3 of which may be linked to a single product. At this time, the FDA and CDC have reported that the outbreak may be linked to Rosabella Moringa Capsules.

We continue to diligently investigate, in collaboration with FDA, this possible link of the Salmonella outbreak to Rosebella Moringa Capsules. We have discontinued use and purchase of all raw moringa leaf powder from the raw material supplier of the above referenced lots.

Customers who have purchased the lots above are asked to dispose of it immediately, do not eat, sell, or serve the product.

Ambrosia Brands is conducting this recall voluntarily and takes this matter very seriously. We apologize for the inconvenience and concern this recall may cause our customers. Our company is committed to ensuring the quality of our products and the well-being of our consumers. Consumers with questions may contact the company M-F from 9am-4pm CT at 914-768-1357.

FDA LINK

Why Not Natural, Houston, Texas, is voluntarily recalling its Why Not Natural Organic Moringa – Green Superfood because they may be contaminated with Salmonella, 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 Moringa Capsules were distributed nationwide through mail orders on Why Not Natural’s e-commerce site and third-party on-line retailers including Amazon.comExternal Link Disclaimer from July 2025 to January 2026.

The product is packaged in a 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.

The potential for contamination was noted by FDA as part of ongoing outbreak investigation of Salmonella in other products containing moringa powder. Distribution and production of the product has been suspended while FDA and Why Not Natural continue their investigation and Why Not Natural has further notified its customers of the recall.

Consumers who have purchased Why Not Natural Moringa Capsules are urged to stop usage and may return them to the company. Consumers may contact Why Not Natural for a full refund or pose questions at care@whynotnatural.com.

FDA Outbreak Advisory

FDA LINK

Gerber Products Company is initiating a voluntary recall of limited batches of Gerber® Arrowroot Biscuits out of an abundance of caution due to the potential presence of soft plastic and/or paper pieces that should not be consumed. The material comes from an arrowroot flour supplier who initiated a recall. We are no longer working with the flour supplier.

This recall is isolated to limited batches of Gerber® Arrowroot Biscuits 5.5oz products produced between July 2025 and September 2025. In the U.S., this recall is nationwide.

No other Gerber® products are impacted by this recall.

Batch codes can be identified on the back of the product packaging. Please utilize reference images below and look for the 10-digit batch code prior to the best before date.

Consumers who may have purchased impacted Gerber® Arrowroot Biscuits should not feed this product to their child and can return the product to the retailer where it was purchased to receive a refund.

While no illnesses or injuries have been reported, we are acting out of an abundance of caution following a recall from the supplier. We are working closely with the U.S. Food & Drug Administration (FDA) and will cooperate fully throughout their review.

The quality, safety and integrity of our products remain our highest priority, and we take this responsibility seriously. We sincerely apologize for any concerns or inconvenience this action causes for parents, caregivers and retail customers.

For consumer support and product questions, Gerber is available 24/7 at 1-800-4-GERBER (1-800-443-7237).

FDA LINK

Superfoods Inc. DBA as Live it Up of New York, New York is recalling all Live it Up Super Greens, including both Original and Wild Berry flavors, with lots beginning with the letter “A” and all stick pack products due to possible contamination with Salmonella, 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 sold to consumers located nationwide in the United States, including Puerto Rico, Guam, and Virgin Islands. Additionally, product was sold to consumers located in the United Kingdom. Products were sold through our direct-to-consumer website since September 2024 and on Amazon.com since July 30, 2025. We are also aware that there may be unauthorized 3rd party distribution to consumers through ebay.com, Walmart.com, or other sites.

The recall includes the following products:

• Live it Up Super Greens, NET WT 8.5oz (240g) with UPC 860013190804
• Live it Up Super Greens, 30 – 0.28oz (8g) sticks, NET WT. 8.47oz (240g) with UPC 850077468063
• Live it Up Super Greens, Wild Berry, NET WT 9.49oz (269.16g), with UPC 860013190811
• Live it Up Super Greens, Wild Berry, 30 – 0.32oz (9g) Sticks, NET WT. 9.52oz (270g), with UPC 850077468070

The recalled products are packaged in green pouches. The lot code is printed on the bottom back of the packaging in black and begins with the letter “A” or the number “3” for a stick pack product. Additionally, the affected product has expiration dates from 08/2026 to 01/2028. Please see the example packaging and lot code below.

To date, there have been 45 illnesses and 12 hospitalizations across the United States due to salmonella contamination linked to a single product. At this time, the FDA and CDC have reported that the outbreak may be linked to Live it Up Super Greens. No other Live it Up products are involved in this recall at this time. Production of the product has been suspended while FDA and the company continue their investigation as to the source of the problem.

Customers who have purchased the affected product are asked to dispose of it immediately, do not eat, sell, or serve the product. Customers may request a refund by contacting Live it Up at recall@artofenso.com and provide your name, order number and a photo of the product with lot codes beginning with “A” and stick pack products.

Live it Up takes food safety extremely seriously. We apologize for the inconvenience and concern this recall may cause our customers. Our company is committed to ensuring the quality of our products and the well-being of our consumers.

FDA Outbreak Advisory

FDA

Superfoods Inc. DBA as Live it Up of New York, New York is recalling all Live it Up Super Greens, including both Original and Wild Berry flavors, with lots beginning with the letter “A” and all stick pack products due to possible contamination with Salmonella, 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 Salmonela 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 sold to consumers located nationwide in the United States, including Puerto Rico, Guam, and Virgin Islands. Additionally, product was sold to consumers located in the United Kingdom. Products were sold through our direct-to-consumer website since September 2024 and on Amazon.com since July 30, 2025. We are also aware that there may be unauthorized 3rd party distribution to consumers through ebay.com, Walmart.com, or other sites.

The recall includes the following products:

• Live it Up Super Greens, NET WT 8.5 oz (240g) with UPC 860013190804.
• Live it Up Super Greens, 30 – 0.28oz (8g) sticks, NET WT. 8.47 oz (240g) with UPC 850077468063
• Live it Up Super Greens, Wild Berry, NET WT 8.5OZ (240g), with UPC 860013190811
• Live it Up Super Greens, Wild Berry, 30 – 0.32oz (9g) Sticks, NET WT. 9.52oz (270g), with UPC 850077468070

The recalled products are packaged in green pouches. The lot code is printed on the bottom back of the packaging in black and begins with the letter “A” or the number “3” for a stick pack product. Additionally, the affected product has expiration dates from 08/2026 to 01/2028. Please see the example packaging and lot code below.

To date, there have been 45 illnesses and 12 hospitalizations across the United States due to salmonella contamination linked to a single product. At this time, the FDA and CDC have reported that the outbreak may be linked to Live it Up Super Greens. No other Live it Up products are involved in this recall at this time. Production of the product has been suspended while FDA and the company continue their investigation as to the source of the problem.

Customers who have purchased the affected product are asked to dispose of it immediately, do not eat, sell, or serve the product. Customers may request a refund by contacting Live it Up at recall@artofenso.com and provide your name, order number and a photo of the product with lot codes beginning with “A” and stick pack products.

Live it Up takes food safety extremely seriously. We apologize for the inconvenience and concern this recall may cause our customers. Our company is committed to ensuring the quality of our products and the well-being of our consumers.

FDA Outbreak Advisory