Cheese Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY & WHEAT. HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 3057
Summary
The FDA issued a Class I for Cheese Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY & WHEAT. HILLSIDE ORCHARD by Hillside Orchard Farms Inc.. Reason: Undeclared egg..
Details
Source
Food Recall
External ID
H-0512-2025
Action Date
2025-08-27
Status
Ongoing
Category
food
Product Description
Cheese Bread Net Wt. 23 oz (652 G) CONTAINS: MILK, SOY & WHEAT. HILLSIDE ORCHARD FARMS 105 Mitcham Circle, Tiger GA 30576
Lot/Code Info: Product #1017 Lot 24323-25197
Quantity Affected: 29cs/12/23oz packages
Reason for Recall
Undeclared egg.
Distribution
Product was shipped to the following states: AL, GA, NC, PA & SC.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-22
Company
Tiger, GA
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 90 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Hillside Orchard Farms Inc. 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 (Hillside Orchard Farms Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hillside Orchard Farms Inc. have FDA actions?
Hillside Orchard Farms Inc. 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 "H-0512-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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