CLASS III Food recall · Reported 11 Jun 2014 · FDA Enforcement Report

Gavina Northwest Blend Dark Whole Bean recalled by F. Gavina & Sons

F. Gavina & Sons is recalling Gavina Northwest Blend Dark Whole Bean, distributed in California, Nebraska. The recall was initiated on 14 May 2014 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot No. 85895
Quantity recalled29 units

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-1985-2014
FDA event ID
68301
Recalling firm
F. Gavina & Sons, Vernon, CA
Classification
Class III
Status
Terminated
Recall initiated
14 May 2014
FDA classified
30 May 2014
Reported
11 Jun 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors
Product category
Beans & Lentils

Timeline

14 May 2014Recall initiated by company
30 May 2014Classified by FDA+16 days
11 Jun 2014Published 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

F. Gavina and Sons Inc. is recalling Gavina Northwest Blend Dark whole beans because it was mislabeled as decaffeinated product.

Product as listed by the FDA

Gavina Northwest Blend Dark Whole Bean Bag Net Wt. 5lb, Product label reads in part "***085895***DECAF EUROPEAN BLEND 5LBS WHOLEBEAN BAG***"

Where it was distributed

CA and NE

CaliforniaNebraska

Questions about this recall

Why was it recalled?

F. Gavina and Sons Inc. is recalling Gavina Northwest Blend Dark whole beans because it was mislabeled as decaffeinated product.

Which lots are affected?

Lot No. 85895

Where was it sold?

CA and NE

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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