Cranberry Chicken Salad Wedge 4.5 oz package in Wedge plastic and clear container with a plastic film sealing the top.
Summary
The FDA issued a Class II for Cranberry Chicken Salad Wedge 4.5 oz package in Wedge plastic and clear containe by FRESHPOINT CENTRAL FLORIDA, INC.. Reason: The chicken salad sandwich has an improperly declared allergen (egg). While egg is included in the ingredients list on the package label, it is not in.
Details
Source
Food Recall
External ID
H-0012-2027
Action Date
2026-10-14
Status
Ongoing
Category
food
Product Description
Cranberry Chicken Salad Wedge 4.5 oz package in Wedge plastic and clear container with a plastic film sealing the top.
Lot/Code Info: Use By Dates from 9/3/2026 to 9/17/2026
Quantity Affected: 1093 units
Reason for Recall
The chicken salad sandwich has an improperly declared allergen (egg). While egg is included in the ingredients list on the package label, it is not included in the allergen Contains statement.
Distribution
Florida and Georgia
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-04
Company
Orlando, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 35 food recalls issued in the same week, part of 92 food-related FDA actions this month.
FRESHPOINT CENTRAL FLORIDA, INC. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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?
FRESHPOINT CENTRAL FLORIDA, INC. 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 "H-0012-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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