RecallHawk
Class I Recall

Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300

FRESHPOINT CENTRAL FLORIDA, INC.

Summary

The FDA issued a Class I for Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300 by FRESHPOINT CENTRAL FLORIDA, INC.. Reason: Mislabeled salads (undeclared peanut allergen). Incorrect ingredient applied (peanuts).

Details

Source

Food Recall

External ID

F-0577-2025

Action Date

2025-03-05

Status

Completed

Category

food

Product Description

Garden Salad 5 oz Lot # 6620223 Best By: 02.05, UPC 766375733300

Lot/Code Info: Lot # 6620223 Best By: 02.05, UPC 766375733300

Quantity Affected: 18 units

Reason for Recall

Mislabeled salads (undeclared peanut allergen). Incorrect ingredient applied (peanuts)

Distribution

Florida and Georgia

Type: Voluntary: Firm initiated

Recall Initiated: 2025-01-28

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 20 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 CENTRAL 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 CENTRAL FLORIDA, INC. have FDA actions?

This is the only FDA action we have on record for FRESHPOINT CENTRAL FLORIDA, INC. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0577-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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