CLASS I RECALLLISTERIA

Member's Mark Freeze-Dried Fruit Recall: Listeria, Sam's Club, Use-By Dates Into 2027

Sam's Club Member's Mark Freeze Dried Fruit Variety Packs (strawberry, banana, apple) were recalled for Listeria. Use-by dates run into July 2027. Check your lot number.

By DeJuan Tartt · Published October 14, 2026 · Fact-checked against FDA records

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The short version

• Doehler Dry Ingredient Solutions, LLC of Cartersville, Georgia recalled Member's Mark Freeze Dried Fruit Variety Pack, 15-count boxes, due to contamination with Listeria monocytogenes, found in the company's routine testing.
• It was sold at Sam's Club stores. FDA's enforcement report lists distribution centers serving 42 states and Puerto Rico, including Oklahoma and Texas.
• Each box holds 5 strawberry, 5 banana and 5 apple pouches.
• The recalled boxes have use-by dates from June 24, 2027 to July 25, 2027. Freeze-dried fruit keeps a long time, so a box bought in summer 2025 may still be in your pantry.
• FDA classified this recall as Class I, its highest-risk recall class.
• The company said no illnesses had been reported when it announced the recall.

Check your box first

Product: Member's Mark Freeze Dried Fruit Variety Pack, 15 count
UPC: 1 93968 50900 2
Where to look: the lot number and use-by date are on the bottom of the case.

That is 22 lots in all. FDA's enforcement report lists 21,552 boxes recalled.

What to do if you have a recalled box

• Do not eat it. The company says: "Consumers who have this product in their possession should not consume the product."
• Throw it away, or take it to any Sam's Club for a full refund.
• Questions: Doehler Dry Ingredient Solutions customer service, 770-387-0451, Monday to Friday, 8 a.m. to 5 p.m. Eastern.

Where it was sold

The product was sold at Sam's Club stores and distributed between July 1 and July 25, 2025. The recall lists these states and territories:

Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Louisiana, Maine, Maryland, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, West Virginia, Wisconsin and Wyoming.

What happened

The company found the problem through its own product testing. It announced the recall on July 30, 2025, and FDA posted the notice on July 31, 2025. FDA classified the recall as Class I on August 6, 2025.

FDA describes Class I as "a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death."

About Listeria

According to the recall notice, Listeria monocytogenes "can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems." Healthy people may have short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. The notice also says Listeria infection "can cause miscarriages and stillbirths among pregnant women."

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