Yellow Squash sold as Bulk recall
Recalled by Southeast Processing Ltd · Forest Park, GA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Finished product samples of half moon sliced yellow squash reported positive for Listeria monocytogenes from third party laboratory.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Yellow Squash sold as Bulk, Diced, Half Moon Sliced, Julienne and Planks (Product codes 168-173)
Quantity: 910lbs
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
..175 06/24/2022/07/02/2022, ..177 06/26/2022/07/04/2022, ..178 06/27/2022/07/05/2022, ..179 06/28/2022/07/06/2022, ..180 06/29/2022/07/07/2022, ..181 06/30/2022/07/08/2022, ..182 07/01/2022/07/09/2022, ..186 07/05/2022/07/13/2022, ..187 07/06/2022/07/14/2022, ..188 07/07/2022/07/15/2022, ..189 07/08/2022/07/16/2022 & ..191 07/11/2022/07/19/2022
Where it was sold
Georgia South Carolina
FDA's distribution note: Product was shipped to GA & SC.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Southeast Processing Ltd
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 6, 2022
- In FDA report of
- Oct 5, 2022
- Terminated
- Feb 24, 2023
- FDA recall number
- F-1793-2022 · event 90575
- Official record
- FDA enforcement report search