BISCUIT MIX, SNG 1000042143 NET WEIGHT 2.625 LBS Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta,
Summary
The FDA issued a Class II for BISCUIT MIX, SNG 1000042143 NET WEIGHT 2.625 LBS Packed Exclusively For: Chick-f by Griffith Foods Inc.. Reason: Undeclared eggs.
Details
Source
Food Recall
External ID
H-0522-2025
Action Date
2025-08-27
Status
Completed
Category
food
Product Description
BISCUIT MIX, SNG 1000042143 NET WEIGHT 2.625 LBS Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, Ga 30349
Lot/Code Info: BEST BY NOV 26, 2025 L 979590 07-29-25
Quantity Affected: 150cs/12/2.625 lb bags
Reason for Recall
Undeclared eggs
Distribution
Product was shipped to two distribution centers, one each in LA & NC.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-10
Company
Alsip, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 90 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Griffith Foods Inc. has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Griffith Foods Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Griffith Foods Inc. have FDA actions?
Griffith Foods Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0522-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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