Member's Mark freeze-dried fruit pouches recalled due to Listeria monocytogenes detected in testing. Consumers should check product dates and avoid using affected items.
Listeria monocytogenes. During routine testing the firm received positive test results for Listeria monocytogenes.
Member's Mark freeze-dried fruit pouches were recalled because testing found Listeria monocytogenes bacteria. This bacteria can cause serious illness, so affected products should not be consumed.
Listeria monocytogenes is a bacteria that can cause severe infections, especially in pregnant women, newborns, the elderly, and those with weakened immune systems. It can lead to miscarriage, stillbirth, severe illness, or death if the bacteria are ingested.
Anyone who owns or has purchased these specific Member's Mark freeze-dried fruit pouches. Pregnant women, newborns, and elderly individuals are at higher risk for serious illness from Listeria.
Check for the following product codes: UPC 1 93968 50900 2, 1 93968 50901 2, 1 93968 50902 2, and other listed UPCs. The best by dates range from June 24, 2027 to July 27, 2027.
Discard any Member's Mark freeze-dried fruit pouches with the listed UPCs and best by dates.
Listeria monocytogenes was detected in routine testing. This bacteria can cause serious illness, especially in pregnant women, newborns, the elderly, and those with weakened immune systems.
Check for the UPC codes listed in the recall: 1 93968 50900 2, 1 93968 50901 2, 1 93968 50902 2, and other listed UPCs with best by dates from June 24, 2027 to July 27, 2027.
Yes, you should stop using and discard any affected products immediately to avoid potential illness.
We’ve drafted a message you can send Member's Mark to request your refund or repair — edit it as you like.
Subject: Recall H-0394-2025 — Member's Mark Member's Mark Hello, I own a Member's Mark that is covered by recall H-0394-2025 from Member's Mark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
