CLASS I Food recall · Reported 26 Dec 2018 · FDA Enforcement Report

Kwik Trip Granola, Bulk Granola recalled by Oakhouse Bakery

Oakhouse Bakery is recalling Kwik Trip Granola, Bulk Granola, 09976, distributed in Wisconsin. The recall was initiated on 27 Nov 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot number OH27118 code date 9/28/19
Quantity recalled8300 lbs.

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-0732-2019
FDA event ID
81648
Recalling firm
Oakhouse Bakery, Madison, WI
Classification
Class I
Status
Terminated
Recall initiated
27 Nov 2018
FDA classified
18 Dec 2018
Reported
26 Dec 2018
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Granola Bars

Timeline

27 Nov 2018Recall initiated by company
18 Dec 2018Classified by FDA+21 days
26 Dec 2018Published 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

Bulk Granola may contain undeclared tree nuts (specifically cashew and almond)

Product as listed by the FDA

Kwik Trip Granola, Bulk Granola, 09976. Net Wt 20 lbs / 9.1 kg. Manufactured by: Oakhouse Bakery, 2221 Mustang Way, Madison, WI 53718.

Where it was distributed

WI only

Wisconsin

Questions about this recall

Why was it recalled?

Bulk Granola may contain undeclared tree nuts (specifically cashew and almond)

Which lots are affected?

Lot number OH27118 code date 9/28/19

Where was it sold?

WI only

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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