CLASS II Food recall · Reported 6 Mar 2019 · FDA Enforcement Report

Craft Granola Goldenola Turmeric & Ginger recalled by Birdseed Food Co

Birdseed Food is recalling Craft Granola Goldenola Turmeric & Ginger, distributed in California, Connecticut, Maryland, New York, Oregon, Pennsylvania. The recall was initiated on 7 Feb 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll expiration dates and includes up to 061419
Quantity recalled440 packages 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-1055-2019
FDA event ID
82107
Recalling firm
Birdseed Food, Bend, OR
Brand
Craft
Classification
Class II
Status
Terminated
Recall initiated
7 Feb 2019
FDA classified
22 Feb 2019
Reported
6 Mar 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Granola Bars

Timeline

7 Feb 2019Recall initiated by company
22 Feb 2019Classified by FDA+15 days
6 Mar 2019Published 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

Craft Granola Goldenola Turmeric & Ginger was recalled due to visible undeclared whole cashews

Product as listed by the FDA

Craft Granola Goldenola Turmeric & Ginger, packaged in 3 oz. and 11 oz. poly bag, UPC: 860157002028 and 8601570020135

Where it was distributed

CA, CT, MD,NY, OR and PA

CaliforniaConnecticutMarylandNew YorkOregonPennsylvania

Questions about this recall

Why was it recalled?

Craft Granola Goldenola Turmeric & Ginger was recalled due to visible undeclared whole cashews

Which lots are affected?

All expiration dates and includes up to 061419

Where was it sold?

CA, CT, MD,NY, OR and PA

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.

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