Deep Chocolate Sheet Cake 8x12 28.125 lb case 20, 22.5 oz cakes per case
⚠ 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-2022-2016.
Products may contain undeclared tree nuts (walnuts). People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2022-2016.
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 Minnie Marie Bakers, Inc. Dba Awrey's Bakery 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-2022-2016.
Minnie Marie Bakers, Inc. dba Awrey's Bakery
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.
Minnie Marie Bakers, Inc. Dba Awrey's Bakery Recall FAQ
Minnie Marie Bakers, Inc. Dba Awrey's Bakery is the subject of a bakery & grains safety report: Deep Chocolate Sheet Cake 8x12 28.125 lb case 20, 22.5 oz cakes per case. The notice was published on July 29, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 560 units are potentially affected.