SunOpta recalls mixed fruit products due to potential Listeria monocytogenes contamination. Consumers should avoid these items if they have the listed lot numbers and best by dates.
Fruit products have the potential to be contaminated with Listeria monocytogenes.
SunOpta is recalling mixed fruit products that may contain Listeria monocytogenes, a bacteria that can cause serious illness. This recall affects products sold with specific lot numbers and best by dates.
Listeria monocytogenes is a bacteria that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. Contamination in these products could lead to illness if eaten.
Anyone who purchased the recalled mixed fruit products from Aldi stores in Batavia, IL. People with weakened immune systems are at higher risk for infection.
Check for lot numbers FMX227603, FMX227604, or FMX227605 with a best by date of October 3, 2024. These products were sold exclusively at Aldi stores in Batavia, IL.
Look for lot numbers FMX227603, FMX227604, or FMX227605 on the packaging.
If you have the recalled lot numbers, discard the products immediately to avoid potential illness.
No, the recalled products may contain Listeria monocytogenes, which can cause serious illness. Do not eat these products.
These products were sold exclusively at Aldi stores in Batavia, IL.
Discard the product immediately if you have lot numbers FMX227603, FMX227604, or FMX227605 with a best by date of October 3, 2024.
We’ve drafted a message you can send SunOpta to request your refund or repair — edit it as you like.
Subject: Recall F-1271-2023 — SunOpta SunOpta Hello, I own a SunOpta that is covered by recall F-1271-2023 from SunOpta. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
