Freshway Foods - Diced Butternut Squash, packaged in 4 pound plastic bags - 4 bags per case.
Summary
The FDA issued a Class I for Freshway Foods - Diced Butternut Squash, packaged in 4 pound plastic bags - 4 ba by Fresh Unlimited Inc. Reason: Potential contamination of Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-1605-2023
Action Date
2023-10-04
Status
Terminated
Category
food
Product Description
Freshway Foods - Diced Butternut Squash, packaged in 4 pound plastic bags - 4 bags per case.
Lot/Code Info: Batch No. 261813, 261919, 261982 Lot No. 2342289, 2371289, 2402289, 2411289, 2421289, 2431289, 2441289 Product No. 75910 Best By: 9/5/23, 9/8/23, 9/11/23, 9/13/23, 9/14/23, 9/15/23, 9/16/23
Quantity Affected: 1,888 pounds
Reason for Recall
Potential contamination of Listeria monocytogenes
Distribution
US Foods Distribution locations: IN, NC, NY, SC, WV
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-06
Company
Sidney, OH
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 185 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 (Fresh Unlimited Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fresh Unlimited Inc have FDA actions?
This is the only FDA action we have on record for Fresh Unlimited Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1605-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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