Parsley bunches Boxes of 30 and 60 count Keep refrigerated SKU 475987 PLU 4899 on twist ties Product of Mexico
Summary
The FDA issued a Class I for Parsley bunches Boxes of 30 and 60 count Keep refrigerated SKU 475987 PLU 4899 o by Church Brothers, LLC. Reason: Parsley imported from Mexico was found to be contaminated with Salmonella.
Details
Source
Food Recall
External ID
F-0310-2023
Action Date
2023-02-01
Status
Terminated
Category
food
Product Description
Parsley bunches Boxes of 30 and 60 count Keep refrigerated SKU 475987 PLU 4899 on twist ties Product of Mexico
Lot/Code Info: GS1 Lot: CB229534
Quantity Affected: 327 cases
Reason for Recall
Parsley imported from Mexico was found to be contaminated with Salmonella
Distribution
Product was distributed to LA, FL, and MI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-23
Company
Salinas, CA
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.
Church Brothers, LLC has 2 FDA actions in our database, including 2 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 (Church Brothers, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Church Brothers, LLC have FDA actions?
Church Brothers, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0310-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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