Boars Head Grab and Go Wedge Ham, Smoke Master Black Forest Ham, Grab and Go Sandwich, NET WT. 7.5 OZ (213 g), Plastic C
Summary
The FDA issued a Class I for Boars Head Grab and Go Wedge Ham, Smoke Master Black Forest Ham, Grab and Go San by Publix Super Markets, Inc.. Reason: Potential Listeria Monocytogenes.
Details
Source
Food Recall
External ID
F-1703-2024
Action Date
2024-08-21
Status
Terminated
Category
food
Product Description
Boars Head Grab and Go Wedge Ham, Smoke Master Black Forest Ham, Grab and Go Sandwich, NET WT. 7.5 OZ (213 g), Plastic Container, KEEP REFRIGERATED
Lot/Code Info: SELL BY 08/01/2024 SELL BY 08/02/2024
Quantity Affected: 2786 units
Reason for Recall
Potential Listeria Monocytogenes
Distribution
U.S. Distribution within the states in retail locations in FL and GA. No Foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-30
Company
Lakeland, 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 125 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 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 (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-1703-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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