PIES & SIDES PUMPKIN PIE 10.5 oz INGREDIENTS: PUMPKIN FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT
Summary
The FDA issued a Class I for PIES & SIDES PUMPKIN PIE 10.5 oz INGREDIENTS: PUMPKIN FILLING, SUGARS, VANILLA, by Robeson Enterprises. Reason: During an inspection by NCDA, the firm was notified that the product contains undeclared milk and eggs. The label fails to list any sub ingredients an.
Details
Source
Food Recall
External ID
F-1143-2024
Action Date
2024-04-17
Status
Ongoing
Category
food
Product Description
PIES & SIDES PUMPKIN PIE 10.5 oz INGREDIENTS: PUMPKIN FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
Lot/Code Info: All lots shipped before 2/23/2024
Quantity Affected: 25 units
Reason for Recall
During an inspection by NCDA, the firm was notified that the product contains undeclared milk and eggs. The label fails to list any sub ingredients and the contain statement does not list milk or eggs.
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-1143-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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