Southeast Processing Ltd recalls yellow squash products (bulk, diced, half moon sliced) sold between June 24-July 19, 2022. Products tested positive for Listeria monocytogenes. Consumers should stop using these items immediately.
Finished product samples of half moon sliced yellow squash reported positive for Listeria monocytogenes from third party laboratory.
Southeast Processing Ltd recalled yellow squash products that tested positive for Listeria monocytogenes. This bacteria can cause serious illness, especially in pregnant women, newborns, and immunocompromised individuals. The recall covers specific product types sold between June 24 and July 19, 2022.
Listeria monocytogenes is a bacterium that can cause serious infections, including meningitis and sepsis. It is particularly dangerous for pregnant women, newborns, and people with weakened immune systems. The bacteria were found in samples of the yellow squash products.
Pregnant women, newborns, and people with weakened immune systems are at highest risk from Listeria infection. Anyone who purchased the recalled yellow squash products between June 24 and July 19, 2022 is affected.
Check for yellow squash sold as bulk, diced, half moon sliced, julienne, or planks. Products with product codes 168-173 were sold between June 24 and July 19, 2022.
Immediately stop using any yellow squash products with product codes 168-173 that were sold between June 24 and July 19, 2022.
Product codes 168-173.
Sold between June 24 and July 19, 2022.
Pregnant women, newborns, and people with weakened immune systems.
We’ve drafted a message you can send Southeast Processing to request your refund or repair — edit it as you like.
Subject: Recall F-1793-2022 — Southeast Processing Southeast Processing Hello, I own a Southeast Processing that is covered by recall F-1793-2022 from Southeast Processing. 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.
