CLASS I Food recall · Reported 14 Jun 2023 · FDA Enforcement Report
Brat Roll Frozen Dough recalled by Gonnella Frozen Products
Gonnella Frozen Products is recalling Brat Roll Frozen Dough, distributed in California, Michigan, Minnesota, Ohio, Utah. The recall was initiated on 15 May 2023 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0973-2023
- FDA event ID
- 92364
- Recalling firm
- Gonnella Frozen Products, Hazle Township, PA
- Brand
- Brat
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 15 May 2023
- FDA classified
- 5 Jun 2023
- Reported
- 14 Jun 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Egg
- Product category
- Bread
Timeline
| 15 May 2023 | Recall initiated by company | |
| 5 Jun 2023 | Classified by FDA | +21 days |
| 14 Jun 2023 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared egg
Product as listed by the FDA
Brat Roll Frozen Dough Product Code 18429 UPC: 00078296184292. Individual unit wt 2.50 oz. Packaged in a cardboard box. 180 pieces per case.
Where it was distributed
Distributed to distributors in MI, MN, OH, UT, and CA.
Questions about this recall
Why was it recalled?
Undeclared egg
Which lots are affected?
Expiration dates 8/22/23, 8/28/23, 9/1/23 302MAY2023; 308MAY2023; 312MAY2023
Where was it sold?
Distributed to distributors in MI, MN, OH, UT, and CA.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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