CLASS I ONGOING Food recall · Reported 19 Apr 2017 · FDA Enforcement Report

7-Eleven, Mantecada Muffin recalled by Bak EZ

Bak EZ is recalling 7-Eleven, Mantecada Muffin, distributed in California, Illinois. The recall was initiated on 24 Feb 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC 05254859241-7, SKU #9841
Quantity recalled2051 cases (123,060 units)

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-1912-2017
FDA event ID
76703
Recalling firm
Bak EZ, Norcross, GA
Classification
Class I
Status
Ongoing
Recall initiated
24 Feb 2017
FDA classified
10 Apr 2017
Reported
19 Apr 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Allergens
Product category
Cakes & Pastries

Timeline

24 Feb 2017Recall initiated by company
10 Apr 2017Classified by FDA+45 days
19 Apr 2017Published 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 Allergen: Milk

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

7-Eleven, Mantecada MUFFIN, Net Wt. 4 oz. , UPC 05254859241-7, in clear flexible plastic, Distributed by 7-Eleven, Inc., Irving, TX 750634.

Where it was distributed

CA and IL

CaliforniaIllinois

Stores named: 7-Eleven

Questions about this recall

Why was it recalled?

Undeclared Allergen: Milk

Which lots are affected?

UPC 05254859241-7, SKU #9841

Where was it sold?

CA and IL

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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