RecallHawk
Class III Recall

PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEA

Robeson Enterprises

Summary

The FDA issued a Class III for PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE FILLING, SUGARS, VANILLA by Robeson Enterprises. Reason: During an inspection by NCDA, the firm was notified that the product label fails to list any sub ingredients..

Details

Source

Food Recall

External ID

F-1145-2024

Action Date

2024-04-17

Status

Ongoing

Category

food

Product Description

PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE 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 label fails to list any sub ingredients.

Distribution

Products were shipped to the following states: GA, NC & SC

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-26

Company

Robeson Enterprises

Mount Holly, NC

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

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 III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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-1145-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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