Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Cod
Summary
The FDA issued a Class I for Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigera by Fresh Express Incorpated. Reason: Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall..
Details
Source
Food Recall
External ID
F-0257-2025
Action Date
2024-12-11
Status
Terminated
Category
food
Product Description
Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Code :71279-56704
Lot/Code Info: Lot Code: Z257, Z262, Z267, Z271 Expiration Date: 09/30/2024, 10/05/2024, 10/10/2024, 10/14/2024
Quantity Affected: 210 Cases
Reason for Recall
Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall.
Distribution
U.S. distribution within states in retail locations in LA, MO, IL, KY, OH, MN, IN, CA, UT, VT, TX, WI. No Foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-18
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 107 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-0257-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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