Fresh EXPRESS Chopped Kit Caesar Romaine Lettuce TOTAL NET WT. 9.4 OZ (266g) SALAD & TOPPINGS: NET WT. 6.9 OZ (196g) DRE
Summary
The FDA issued a Class I for Fresh EXPRESS Chopped Kit Caesar Romaine Lettuce TOTAL NET WT. 9.4 OZ (266g) SAL by Fresh Express Incorpated. Reason: The firm was notified by one of their customers that their product test positive for Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0753-2023
Action Date
2023-05-03
Status
Terminated
Category
food
Product Description
Fresh EXPRESS Chopped Kit Caesar Romaine Lettuce TOTAL NET WT. 9.4 OZ (266g) SALAD & TOPPINGS: NET WT. 6.9 OZ (196g) DRESSING 2.5 fl. oz. (74 mL)/NET WT 2.5 oz. (71g) fresh express incorporated P.O. BOX 80599, SALINAS, CA 93912 UPC 0 71279 30919 4
Lot/Code Info: G075/ 04/02/23
Quantity Affected: 3,333cs/6/9.4oz bags
Reason for Recall
The firm was notified by one of their customers that their product test positive for Listeria monocytogenes.
Distribution
Product was shipped to the following states: FL, GA, NC, SC, VA
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-07
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 28 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-0753-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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