- FDA recalls multiple greens powders sold nationwide due to Salmonella contamination.
- 11 illnesses and three hospitalizations reported; products were sold at Sam’s Club, Amazon and more.
- Consumers should discard recalled powders and contact a healthcare provider if experiencing symptoms.
The U.S. Food and Drug Administration (FDA) just announced a Salmonella outbreak linked to multiple brands of greens powder. The products affected were sold at Sam’s Club stores nationwide as well as online through Amazon, eBay, Etsy, Target, Walmart and more.
The following products have been connected to this outbreak and are being recalled, including affected sizes and lot codes:
- Food To Live Organic Moringa Leaf Powder in 8-ounce, 1-pound, 2-pound, 4-pound, 8-pound, 16-pound and 44-pound bags with lot codes “SO-69006” through “SO-72558.”
- Food To Live Organic Supergreens Powder Mix in 8-ounce, 1-pound, 1.5-pound, 3-pound, 6-pound and 12-pound bags with lot codes “SO-69006” through “SO-72558.”
- Organic Moringa Leaf Powder in a 1-kilogram box sold on Africa Imports’ website (africaimports.com) after June 5.
- All Member’s Mark Super Greens dietary supplement powder, regardless of lot codes and best-by dates.
Check your greens powder, and if it matches any of the above recalled products, dispose of it immediately or return to your place of purchase for a refund. As of November 13, there have been 11 illnesses, including three hospitalizations, connected to the consumption of impacted greens powders. While the products were distributed nationwide, the outbreak has directly impacted the following states: Florida, Kansas, Michigan, New York, North Carolina, South Carolina and Virginia.
Symptoms of Salmonella infection (salmonellosis) can start from six hours to six days after infection, and they can last up to seven days. Common signs of salmonellosis include watery or bloody diarrhea, stomach cramps, headache, nausea, vomiting and loss of appetite. If you are experiencing any of these symptoms after taking greens powder, consult a healthcare professional immediately.
This investigation is ongoing and more products may be affected. For questions about this outbreak, contact the FDA at 1-888-INFO-FDA (1-888-463-6332).
