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orywireThe FDA-posted recall expansion adds more TNVitamins and Doctor’s Pride moringa capsule lots to a Salmonella-related recall list. CDC also lists a separate MOGO moringa-capsule outbreak, and consumers should check lot numbers before using any recalled product.
The FDA-posted moringa supplement recall has expanded, and federal health officials are urging consumers to check bottles and pouches of several moringa-containing dietary supplements for Salmonella-related recall details. The latest FDA update adds more TNVitamins and Doctor’s Pride moringa capsule lots to the recall list, while the Centers for Disease Control and Prevention says it is investigating two Salmonella outbreaks linked to moringa products.
The U.S. Food and Drug Administration said June 3 that Total Nutrition Inc. of Deer Park, New York, expanded its recall of TNVitamins and Doctor’s Pride moringa capsules. The newly added lot is 2748, with an expiration date of 07/2027, for both TNVitamins Ultra Potent Complete Green Superfood Moringa 10,000 mg and Doctor’s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg, both sold in 120-capsule bottles.
CDC’s latest accessible outbreak page, dated May 27, listed 119 illnesses, 32 hospitalizations and no deaths across 36 states in the reopened moringa leaf powder outbreak. CDC also lists a separate MOGO moringa-capsule outbreak with 18 illnesses, seven hospitalizations and no deaths across 14 states.
FDA and CDC reopened a multistate outbreak investigation involving Salmonella Typhimurium and Salmonella Newport infections linked to dietary supplements containing imported moringa leaf powder after new illnesses and exposure information were reported. The investigation had previously been closed on March 17, but FDA said 22 new illnesses from four states were later added.
Total Nutrition first recalled certain TNVitamins and Doctor’s Pride moringa capsule lots on May 26. In a company announcement posted by FDA, Total Nutrition said the June 2 expansion followed a traceability review that identified a common raw material from one of the original recalled lots.
Separately, FDA and CDC are investigating a May 2026 outbreak linked to MOGO-brand Pure Moringa Oleifera capsules.
Recalled TNVitamins Ultra Potent Complete Green Superfood Moringa 10,000 mg, 120 capsules, now includes lots 2507199 with expiration 09/2027, 2512-304 with expiration 02/2028, 2793 with expiration 02/2028 and 2748 with expiration 07/2027. The accessible FDA expansion notice did not list a UPC for this product.
Recalled Doctor’s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg, 120 capsules, includes lot 2507199 with expiration 09/2027 and lot 2748 with expiration 07/2027. The accessible FDA expansion notice did not list a UPC for this product.
FDA also lists recalled Why Not Natural Pure Organic Moringa Green Superfood capsules, lot A25G051 with expiration 07/2028, and recalled Live it Up Super Greens dietary supplement powders, including original and wild berry products with affected expiration dates from 08/2026 to 01/2028.
In the separate MOGO outbreak, recalled MOGO Pure Moringa Oleifera Capsules include UPC 636339970617, lot 15525AA with expiration 06/2027 and lot 00926AA with expiration 01/2028.
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Several POM power bank lines sold in TK Maxx and Homesense stores are being recalled over a fire risk linked to internal wiring. Owners should stop using affected models immediately and return them for a refund or replacement.
FDA says the Total Nutrition investigation is ongoing. The agency said it is conducting additional traceback of the supply chain and working with state and local partners to sample products and determine whether additional products may be contaminated.
For the MOGO investigation, FDA said it is conducting traceback and working with state partners to collect samples. The agencies have not announced a final source of contamination for either active investigation.
FDA says consumers and retailers should not eat, sell or distribute recalled TNVitamins, Doctor’s Pride, Why Not Natural, Live it Up or MOGO moringa products. Total Nutrition said it has stopped distribution and sale of the identified products and started removal orders across applicable sales and fulfillment channels.
CDC advises consumers not to eat recalled products, to throw them away or return them where purchased, and to wash items and surfaces that may have touched recalled supplements with hot soapy water or in a dishwasher.
The reopened FDA/CDC investigation covers 119 confirmed illnesses in 36 states, with 32 hospitalizations and no reported deaths. Illness onset dates in that investigation range from August 22, 2025, to April 26, 2026, according to FDA.
The separate MOGO investigation covers 18 illnesses in 14 states, with seven hospitalizations and no reported deaths. FDA lists the last illness onset in that investigation as April 7, 2026.
Consumers should check the product name, lot code and expiration date before using any moringa supplement. If the product matches a recalled lot, do not use it. FDA and CDC advise throwing away recalled products and cleaning surfaces or containers that may have touched them.
CDC says consumers should call a health care provider right away for diarrhea with a fever higher than 102 degrees, diarrhea lasting more than two days without improvement, bloody diarrhea, repeated vomiting that prevents keeping liquids down, or signs of dehydration. CDC says Salmonella symptoms often include diarrhea, fever and stomach cramps and usually begin six hours to six days after swallowing the bacteria.
Moringa leaf powder has been tied to several Salmonella-related supplement recalls and outbreak investigations since 2025. FDA’s current January 2026 moringa leaf powder advisory includes the latest Total Nutrition expansion and earlier recalled Live it Up and Why Not Natural products. FDA and CDC also maintain a separate May 2026 advisory for MOGO moringa capsules.
Because these supplements can have long shelf lives, recalled products may still be in homes even if they are no longer available for sale.
This article was prepared after a live review of FDA and CDC outbreak pages and recall notices on June 3, 2026. It should be updated if FDA or CDC changes case counts, adds recalled products, adds UPCs or lot codes, or closes either active investigation.
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