EGG CUSTARD PIE, NET WT 25 OZ (1 LB 9 OZ) 709 g, packaged in paper carton with plastic film window, 6 cartons per case.
Summary
The FDA issued a Class II for EGG CUSTARD PIE, NET WT 25 OZ (1 LB 9 OZ) 709 g, packaged in paper carton with p by Publix Super Markets, Inc.. Reason: Undeclared Tree Nut (Coconut).
Details
Source
Food Recall
External ID
F-0655-2024
Action Date
2024-01-03
Status
Terminated
Category
food
Product Description
EGG CUSTARD PIE, NET WT 25 OZ (1 LB 9 OZ) 709 g, packaged in paper carton with plastic film window, 6 cartons per case.
Lot/Code Info: Coconut Custard Pie master case (shipped frozen) was labeled with expiration date of Feb-26-2024, Lot #: 101923B1. Individual pie cartons were labeled with a 3-day shelf life at the retail stores when placed on refrigerated display for sale (thawed). Dates on individual pie cartons offered for sale to customers may range from sell by date of 10/22/23 through sell by date of 11/18/23.
Quantity Affected: 1,100 cases containing 6 pies in each case.
Reason for Recall
Undeclared Tree Nut (Coconut)
Distribution
Domestic distribution only within state of Florida.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-16
Company
Lakeland, 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 59 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Publix Super Markets, Inc. has 10 FDA actions in our database, including 10 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 (Publix Super Markets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Publix Super Markets, Inc. have FDA actions?
Publix Super Markets, Inc. 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-0655-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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