CLASS I Food recall · Reported 12 Dec 2018 · FDA Enforcement Report

Telera and Bolillo Mexican White Bread and per pkg recalled

Tres Hermanos Bakery is recalling Telera and Bolillo Mexican White Bread and per pkg, distributed in Michigan. The recall was initiated on 24 Nov 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesExp. date range from NOV 20 2018 thru DEC 19 2018
Quantity recalled800 packages

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-0749-2019
FDA event ID
81634
Recalling firm
Tres Hermanos Bakery, Wyoming, MI
Brand
Telera
Classification
Class I
Status
Terminated
Recall initiated
24 Nov 2018
FDA classified
21 Dec 2018
Reported
12 Dec 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Bread

Timeline

24 Nov 2018Recall initiated by company
12 Dec 2018Published in enforcement report+18 days
21 Dec 2018Classified by FDA+9 days

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

Reason for recall

Tres Hermanos Bakery initiated a voluntary recall of Telera and Bolillo due to undeclared allergen milk.

Product as listed by the FDA

Tres Hermanos Bakery Telera and Bolillo Mexican White Bread, 1lb and 2 ounces per pkg

Where it was distributed

Finished product is only distributed in Western MI

Michigan

Questions about this recall

Why was it recalled?

Tres Hermanos Bakery initiated a voluntary recall of Telera and Bolillo due to undeclared allergen milk.

Which lots are affected?

Exp. date range from NOV 20 2018 thru DEC 19 2018

Where was it sold?

Finished product is only distributed in Western MI

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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