BrightFarms Lakeside Crunch; packaged in clear, plastic clamshell; 4oz; grown at the company's Rochelle, Illinois indoor
Summary
The FDA issued a Class I for BrightFarms Lakeside Crunch; packaged in clear, plastic clamshell; 4oz; grown at by Bright Farms. Reason: Product may be contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-0892-2021
Action Date
2021-09-08
Status
Terminated
Category
food
Product Description
BrightFarms Lakeside Crunch; packaged in clear, plastic clamshell; 4oz; grown at the company's Rochelle, Illinois indoor farm
Lot/Code Info: UPC: 5706200479 Best By Dates through 7/29/2021
Quantity Affected: N/A
Reason for Recall
Product may be contaminated with Salmonella.
Distribution
IL, WI, IA, IN, MI
Type: Voluntary: Firm initiated
Recall Initiated: 2021-07-15
Company
New York, 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 57 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Bright Farms has 10 FDA actions in our database, including 10 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 (Bright Farms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bright Farms have FDA actions?
Bright Farms has 10 FDA actions in our database, including 10 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0892-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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