"Lettuce Trio" (salad product) packed in 9oz. packages
Summary
The FDA issued a Class I for "Lettuce Trio" (salad product) packed in 9oz. packages by Fresh Express Inc (Div of Chiquita Brands). Reason: potential to be contaminated with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0569-2022
Action Date
2022-02-02
Status
Terminated
Category
food
Product Description
"Lettuce Trio" (salad product) packed in 9oz. packages
Lot/Code Info: Z324-Z350
Quantity Affected: 3,009 cases
Reason for Recall
potential to be contaminated with Listeria monocytogenes
Distribution
Products were distributed to 110 domestic distributors (in CT, IA, IL, IN, KY, MA, MD, ME, MI, MN, MO, ND, NH, NJ, NY, OH, PA, RI, VA, and WI) and 3 foreign distributors (Canada).
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-18
Company
Streamwood, IL
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 117 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Fresh Express Inc (Div of Chiquita Brands) has 90 FDA actions in our database, including 90 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 Inc (Div of Chiquita Brands)) 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 Inc (Div of Chiquita Brands) have FDA actions?
Fresh Express Inc (Div of Chiquita Brands) has 90 FDA actions in our database, including 90 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0569-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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