Gourmet Foods Mamma-Italia Traditional Italian Raw Pizza Dough Ball, Box Quantity: 30 16 oz BALL Keep Frozen NET WT: 30 lbs (13.61Kg), I...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1924-2015.
During an inspection by the Ohio Department of Agriculture, the firm was notified that their labels lack the declaration of "Milk"
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1924-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Dough Acquisition Co or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1924-2015.
Dough Acquisition Co
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Dough Acquisition Co Recall FAQ
Dough Acquisition Co is the subject of a frozen food safety report: Gourmet Foods Mamma-Italia Traditional Italian Raw Pizza Dough Ball, Box Quantity: 30 16 oz BALL Keep Frozen NET WT: 30 lbs (13.61Kg), I.... The notice was published on February 25, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 780 units are potentially affected.