CLASS I Food recall · Reported 21 Sep 2016 · FDA Enforcement Report

AZ House Granola recalled by Mount Franklin Foods

Mount Franklin Foods is recalling AZ House Granola, distributed in Illinois, Texas, Wisconsin. The recall was initiated on 28 Jul 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes16181, 16182, 16189, 16202
Quantity recalled2071 cases

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-2089-2016
FDA event ID
74831
Recalling firm
Mount Franklin Foods, El Paso, TX
Classification
Class I
Status
Terminated
Recall initiated
28 Jul 2016
FDA classified
13 Sep 2016
Reported
21 Sep 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Peanuts
Product category
Granola Bars

Timeline

28 Jul 2016Recall initiated by company
13 Sep 2016Classified by FDA+47 days
21 Sep 2016Published in enforcement report+8 days

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

Reason for recall

Undeclared peanuts, almonds and milk

Product as listed by the FDA

AZ House Granola MANUFACTURED BY: Azar Nut Company El Paso, TX 79912 packaged in 5 pound plastic bags; 1 case containing one 5 pound bag

Where it was distributed

TX, IL, and WI

IllinoisTexasWisconsin

Questions about this recall

Why was it recalled?

Undeclared peanuts, almonds and milk

Which lots are affected?

16181, 16182, 16189, 16202

Where was it sold?

TX, IL, and WI

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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