SunOpta recalls 32oz tropical fruit blends due to potential Listeria monocytogenes contamination. Consumers should check lot numbers on packaging for affected items sold by Aldi in Batavia, IL.
Fruit products have the potential to be contaminated with Listeria monocytogenes.
SunOpta is recalling tropical fruit blends that may contain Listeria monocytogenes, a bacteria that can cause serious foodborne illness. This recall affects specific lot numbers sold through Aldi stores in Batavia, Illinois.
Listeria monocytogenes is a bacteria that can cause severe food poisoning, especially in pregnant people, newborns, and those with compromised immune systems. This product was found to have the potential for contamination with this bacteria, though the actual risk level is low based on the recall.
Anyone who purchased the 32-ounce tropical fruit blend from Aldi stores in Batavia, Illinois between October 2024 and February 2025. Pregnant individuals and those with weakened immune systems are at higher risk for serious illness.
Check for lot numbers starting with FMX followed by 6 digits (e.g., FMX227703) on the packaging. The product was sold by Aldi in Batavia, Illinois from October 2024 through February 2025.
Look for lot numbers on the packaging that start with FMX followed by 6 digits, such as FMX227703.
If your product has a lot number in the list provided, discard it immediately to avoid potential illness.
The product may contain Listeria monocytogenes, which can cause serious illness, but the risk level is low. Only products with specific lot numbers listed in the recall are affected.
This product was sold exclusively by Aldi stores in Batavia, Illinois.
Check the lot number on the packaging. If it starts with FMX followed by 6 digits (e.g., FMX227703), it is part of the recall.
We’ve drafted a message you can send SunOpta to request your refund or repair — edit it as you like.
Subject: Recall F-1270-2023 — SunOpta SunOpta Hello, I own a SunOpta that is covered by recall F-1270-2023 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.
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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.
