CLASS I Food recall · Reported 18 Feb 2015 · FDA Enforcement Report

Twix Bismark recalled by Northern Tier Bakery (

Northern Tier Bakery ( is recalling Twix Bismark, distributed in Minnesota, Wisconsin. The recall was initiated on 15 Jan 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduct distributed January 1, 2015 to January 14, 2015.
Quantity recalled6247

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-1194-2015
FDA event ID
70295
Recalling firm
Northern Tier Bakery (, St Paul Park, MN
Classification
Class I
Status
Terminated
Recall initiated
15 Jan 2015
FDA classified
11 Feb 2015
Reported
18 Feb 2015
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Undeclared Peanuts
Product category
Other

Timeline

15 Jan 2015Recall initiated by company
11 Feb 2015Classified by FDA+27 days
18 Feb 2015Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Northern Tier Bakery LLC dba Supermom's Bakery is recalling Twix Bismarcks because the Twix Chopped Topping might contain undeclared peanuts.

Product as listed by the FDA

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 K and Marathon Stores.

Where it was distributed

WI & MN

MinnesotaWisconsin

Questions about this recall

Why was it recalled?

Northern Tier Bakery LLC dba Supermom's Bakery is recalling Twix Bismarcks because the Twix Chopped Topping might contain undeclared peanuts.

Which lots are affected?

Product distributed January 1, 2015 to January 14, 2015.

Where was it sold?

WI & MN

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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