PIES & SIDES MO' MONEY PIE INGREDIENTS: BLACK EYED PEAS, COLLARDS, ELBOW PASTA, CHEESES, CORNMEAL, BLEACHED FLOUR, MILK
Summary
The FDA issued a Class I for PIES & SIDES MO' MONEY PIE INGREDIENTS: BLACK EYED PEAS, COLLARDS, ELBOW PASTA, by Robeson Enterprises. Reason: During an inspection by NCDA, the firm was notified that the label fails to declare the allergen soy as an ingredient. The firm was also notified that.
Details
Source
Food Recall
External ID
F-1140-2024
Action Date
2024-04-17
Status
Ongoing
Category
food
Product Description
PIES & SIDES MO' MONEY PIE INGREDIENTS: BLACK EYED PEAS, COLLARDS, ELBOW PASTA, CHEESES, CORNMEAL, BLEACHED FLOUR, MILK PRODUCTS, SPICES. CONTAINS: MILK, EGG, WHEAT PIES & SIDES MOUNT HOLLY, NC
Lot/Code Info: All lots shipped before 2/23/2024
Quantity Affected: 244 units
Reason for Recall
During an inspection by NCDA, the firm was notified that the label fails to declare the allergen soy as an ingredient. The firm was also notified that the label does not list any sub ingredients or the allergen soy in the contains statement.
Distribution
Products were shipped to the following states: GA, NC & SC
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-26
Company
Mount Holly, NC
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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Robeson Enterprises has 14 FDA actions in our database, including 14 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 (Robeson Enterprises) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Robeson Enterprises have FDA actions?
Robeson Enterprises has 14 FDA actions in our database, including 14 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1140-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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