Yellow Squash sold as Bulk, Diced, Half Moon Sliced, Julienne and Planks (Product codes 168-173)
Summary
The FDA issued a Class I for Yellow Squash sold as Bulk, Diced, Half Moon Sliced, Julienne and Planks (Produc by Southeast Processing Ltd. Reason: Finished product samples of half moon sliced yellow squash reported positive for Listeria monocytogenes from third party laboratory..
Details
Source
Food Recall
External ID
F-1793-2022
Action Date
2022-10-05
Status
Terminated
Category
food
Product Description
Yellow Squash sold as Bulk, Diced, Half Moon Sliced, Julienne and Planks (Product codes 168-173)
Lot/Code Info: ..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
Quantity Affected: 910lbs
Reason for Recall
Finished product samples of half moon sliced yellow squash reported positive for Listeria monocytogenes from third party laboratory.
Distribution
Product was shipped to GA & SC.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-06
Company
Forest Park, GA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 76 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Southeast Processing Ltd) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Southeast Processing Ltd have FDA actions?
This is the only FDA action we have on record for Southeast Processing Ltd in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1793-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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