Brat Roll Frozen Dough Product Code 18429 UPC: 00078296184292. Individual unit wt 2.50 oz. Packaged in a cardboard box.
Summary
The FDA issued a Class I for Brat Roll Frozen Dough Product Code 18429 UPC: 00078296184292. Individual unit w by Gonnella Frozen Products, LLC. Reason: Undeclared egg.
Details
Source
Food Recall
External ID
F-0973-2023
Action Date
2023-06-14
Status
Terminated
Category
food
Product Description
Brat Roll Frozen Dough Product Code 18429 UPC: 00078296184292. Individual unit wt 2.50 oz. Packaged in a cardboard box. 180 pieces per case.
Lot/Code Info: Expiration dates 8/22/23, 8/28/23, 9/1/23 302MAY2023; 308MAY2023; 312MAY2023
Quantity Affected: 949 cases
Reason for Recall
Undeclared egg
Distribution
Distributed to distributors in MI, MN, OH, UT, and CA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-15
Company
Hazle Township, PA
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Gonnella Frozen Products, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Gonnella Frozen Products, LLC have FDA actions?
This is the only FDA action we have on record for Gonnella Frozen Products, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0973-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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