CLASS II Food recall · Reported 30 Jun 2021 · FDA Enforcement Report

O'Brien's Own Gourmet Granola, busy bee's honey & oat recalled

Browns Granola is recalling O'Brien's Own Gourmet Granola, busy bee's honey & oat, distributed in Iowa. The recall was initiated on 2 Jun 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesall best buy dates
Quantity recalled282 bags (total)

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-0680-2021
FDA event ID
88059
Recalling firm
Browns Granola, Center Point, IA
Classification
Class II
Status
Terminated
Recall initiated
2 Jun 2021
FDA classified
18 Jun 2021
Reported
30 Jun 2021
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Granola Bars

Timeline

2 Jun 2021Recall initiated by company
18 Jun 2021Classified by FDA+16 days
30 Jun 2021Published in enforcement report+12 days

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

Reason for recall

Three flavors of 3X Protein granola are labeled to contain whey, but do not declare milk on the label.

Product as listed by the FDA

O'Brien's Own Gourmet Granola, busy bee's honey & oat, Net Wt. 12 OZ , UPC 6 09132 49667 7; Manufactured and Distributed by O'Brien's Own Gourmet Granola, Center Point, IA.

Where it was distributed

Distributed to grocery stores in Iowa and directly to consumers at farmer's markets.

Iowa

Questions about this recall

Why was it recalled?

Three flavors of 3X Protein granola are labeled to contain whey, but do not declare milk on the label.

Which lots are affected?

all best buy dates

Where was it sold?

Distributed to grocery stores in Iowa and directly to consumers at farmer's markets.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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.

Other products in this recall event

2 other products · FDA event 88059

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