Chopped Salad Kit Southwest with condiments(toppings that include cheese), labeled salad bag (Green Cabbage, Green Leaf
Summary
The FDA issued a Class I for Chopped Salad Kit Southwest with condiments(toppings that include cheese), label by Fresh Express Incorpated. Reason: Product has the potential to be contaminated with Listeria monocytogenes. The condiment pack in the salad kit contains cheese recalled by the cheese .
Details
Source
Food Recall
External ID
F-0875-2024
Action Date
2024-02-21
Status
Terminated
Category
food
Product Description
Chopped Salad Kit Southwest with condiments(toppings that include cheese), labeled salad bag (Green Cabbage, Green Leaf Lettuce, Kale, Red Cabbage, Carrots, Green Onions, Tortilla Strips, Cheddar Cheese, and Chipotle Ranch Dressing), Net Wt 13.4 oz, 6 bags per case. UPC 681131305129
Lot/Code Info: Lot Number:G002 Expiration/Use By Date :2024-01-17 Lot Number:G364 Expiration/Use By Date :2024-01-14 Condiment Pack Use-by Dates 03/03/2024
Quantity Affected: 878 cases
Reason for Recall
Product has the potential to be contaminated with Listeria monocytogenes. The condiment pack in the salad kit contains cheese recalled by the cheese supplier.
Distribution
AL, FL, GA, CA, UT, WA; Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-08
Company
Windermere, FL
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 60 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Fresh Express Incorpated has 9 FDA actions in our database, including 9 recalls.
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 Express Incorpated) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fresh Express Incorpated have FDA actions?
Fresh Express Incorpated has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0875-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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