Twix Bismark. This is not a packaged item. Twix Bismarcks are produced daily to be sold in bakery display cases at certain SA, BP, Circle...
⚠ 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-1194-2015.
Northern Tier Bakery LLC dba Supermom's Bakery is recalling Twix Bismarcks because the Twix Chopped Topping might contain undeclared peanuts.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1194-2015.
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 Northern Tier Bakery (dba\ Super Mom's) 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-1194-2015.
Northern Tier Bakery (dba\ Super Mom's)
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.
Northern Tier Bakery (dba\ Super Mom's) Recall FAQ
Northern Tier Bakery (dba\ Super Mom's) is the subject of a produce safety report: Twix Bismark. This is not a packaged item. Twix Bismarcks are produced daily to be sold in bakery display cases at certain SA, BP, Circle.... The notice was published on January 15, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 6,247 units are potentially affected.