Gavina Northwest Blend Coffee – Mislabeling (2014)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Gavina Northwest Blend Dark Whole Bean Bag Net Wt. 5lb, Product label reads in part "***085895***DECAF EUROPEAN BLEND 5LBS WHOLEBEAN BAG***"
Brand
F. Gavina & Sons Inc.
Lot Codes / Batch Numbers
Lot No. 85895
Products Sold
Lot No. 85895
F. Gavina & Sons Inc. is recalling Gavina Northwest Blend Dark Whole Bean Bag Net Wt. 5lb, Product label reads in part "***085895** due to F. Gavina and Sons Inc. is recalling Gavina Northwest Blend Dark whole beans because it was mislabeled as decaffeinated product.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
F. Gavina and Sons Inc. is recalling Gavina Northwest Blend Dark whole beans because it was mislabeled as decaffeinated product.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, NE
Page updated: Jan 6, 2026