FC Parsley Curly Chopped Fine,12 Count, 2 1.5 Refrigerated at 34F, 301193, UPC 10022363, Parsley 12 CT, DIST BY FPSF, 2
Summary
The FDA issued a Class I for FC Parsley Curly Chopped Fine,12 Count, 2 1.5 Refrigerated at 34F, 301193, UPC by FreshPoint South Florida, Inc.. Reason: Parsley imported from Mexico was found to be contaminated with Salmonella.
Details
Source
Food Recall
External ID
F-0311-2023
Action Date
2023-02-01
Status
Terminated
Category
food
Product Description
FC Parsley Curly Chopped Fine,12 Count, 2 1.5 Refrigerated at 34F, 301193, UPC 10022363, Parsley 12 CT, DIST BY FPSF, 22363 LOC 51, Parsley 6 CT, DIST BY FPSF, 22363 LOC 51
Lot/Code Info: JULIAN DATES FROM 346 TO 354
Quantity Affected: 1,269 cases
Reason for Recall
Parsley imported from Mexico was found to be contaminated with Salmonella
Distribution
FL
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-23
Company
Pompano Beach, 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 57 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 (FreshPoint South Florida, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FreshPoint South Florida, Inc. have FDA actions?
This is the only FDA action we have on record for FreshPoint South Florida, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0311-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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