Fairhope Roasting Company Cold Brew Coffee Concentrate

Fairhope Roasting Company has recalled Fairhope Roasting Company Cold Brew Coffee Concentrate, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 24, 2026 and was initiated on May 21, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Fairhope Roasting Company Cold Brew Coffee Concentrate, with approximately 15 gallons affected. The company behind the recall is Fairhope Roasting Company, based in Fairhope, AL. The FDA describes the product as: “Fairhope Roasting Company Cold Brew Coffee Concentrate, packaged in 1-gallon plastic jugs, UPC 852236006062, for food service only”

Why was Fairhope Roasting Company Cold Brew Coffee Concentrate recalled?

According to the FDA, the stated reason for the recall is: “Product requires refrigeration but the label is missing a "Keep Refrigerated" statement.”

What should you do?

If you think you may have bought Fairhope Roasting Company Cold Brew Coffee Concentrate, compare it against the product description and identifying codes (Batch Number: 05/11/26, Expiration Date: 09/09/26 Batch Number: 05/12/26, Expiration Date: 09/10/26 Batch Number: 05/13/26, Expiration Date: 09/11/26 Batch Num…) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Fairhope Roasting Company or your local health authority.

About this recall

This recall was distributed in AL. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.