BrightFarms Southwest Chipotle Salad Kit Ready to eat salad kit containing green lettuce (grown by indoors at BrightFar
Summary
The FDA issued a Class I for BrightFarms Southwest Chipotle Salad Kit Ready to eat salad kit containing gree by BrightFarms. Reason: Product ingredient may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1065-2024
Action Date
2024-03-20
Status
Terminated
Category
food
Product Description
BrightFarms Southwest Chipotle Salad Kit Ready to eat salad kit containing green lettuce (grown by indoors at BrightFarms) and a master pack supplied by Latitude 36 Foods, which contain cotija cheese, dressing and toppings. Intended for retail distribution to consumers. Cotija Cheese is manufactured by Rizo Lopez Foods Inc.
Lot/Code Info: Best by dates Dec. 31, 2023 through Feb. 22, 2024 2.3 - UPC Codes: 8-50051-82500-4
Quantity Affected: 24960 units
Reason for Recall
Product ingredient may be contaminated with Listeria monocytogenes.
Distribution
Delaware, Maryland, Maine, Massachusetts, New Hampshire, New Jersey, New York, North Carolina, Pennsylvania, Vermont, Virginia, and Washington D.C
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-07
Company
Irvington, NY
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 52 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 (BrightFarms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BrightFarms have FDA actions?
This is the only FDA action we have on record for BrightFarms in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1065-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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