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Lower risk Food recall · FDA · Published May 21, 2026

Fairhope Cold Brew Coffee Concentrate: Missing 'Keep Refrigerated' Label

Fairhope Roasting Company recalls cold brew coffee concentrate jugs due to missing refrigeration label. This could cause spoilage if stored at room temperature.

🇺🇸 FDA recall #H-0951-2026FoodFairhope Roasting Company ›
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Recalling firmFairhope Roasting Company759 Nichols Ave · Fairhope, AL 36532-1768
✎ GovInfoNow plain-language explainer

Fairhope Roasting Company is recalling cold brew coffee concentrate jugs because the label doesn't say 'Keep Refrigerated'. This means the coffee could spoil if left out of the fridge, but it won't cause injury. Read more at govinfonow.com/recall/6209-fairhope-cold-brew-coffee-concentrate-missing-keep-refrigerated-label.

Source Summary by GovInfoNow · govinfonow.com/recall/6209-fairhope-cold-brew-coffee-concentrate-missing-keep-refrigerated-label · Updated August 9, 2026 · Official notice: FDA #H-0951-2026

Cite this page

“Fairhope Cold Brew Coffee Concentrate: Missing 'Keep Refrigerated' Label.” GovInfoNow, updated August 9, 2026. https://govinfonow.com/recall/6209-fairhope-cold-brew-coffee-concentrate-missing-keep-refrigerated-label. Based on FDA recall #H-0951-2026.

The FDA announced on May 21, 2026, that Fairhope Roasting Company is recalling Cold Brew Coffee Concentrate because the label lacks a required "Keep Refrigerated" statement. The agency said the product requires refrigeration to remain safe for consumption.

How to tell if you have it

  • Fairhope Roasting Company Cold Brew Coffee Concentrate
  • 1-gallon plastic jugs
  • UPC 852236006062
  • 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 Number: 05/14/26, Expiration Date: 09/12/26

The hazard

The FDA said the product requires refrigeration but the label is missing a "Keep Refrigerated" statement. The agency classified the recall as Class II.

How to tell if you have this one

Check for 1-gallon plastic jugs with UPC 852236006062. The product was sold with batch numbers from 05/11/26 to 05/14/26 and expires by 09/09/26 to 09/12/26.

  • Brand
    Fairhope Roasting Company
  • Product
    Fairhope Roasting Company Cold Brew Coffee Concentrate, packaged in 1-gallon plastic jugs, UPC 852236006062, for food
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Refrigeration Status

    If the coffee concentrate is stored at room temperature, it may have spoiled. Refrigerate it immediately if not already kept cold.

Where it went and when

Where it was distributed

Distributed in Alabama.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: yesALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Product distributed in AL for food service only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama.

Recall timeline

FDA terminated this recall 48 days after the firm started it.

1. Firm started the recall: May 21, 202612. FDA classified it Class II: Jun 18, 202623. Published in FDA’s Enforcement Report: Jun 24, 202634. FDA terminated the recall: Jul 8, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0951-2026 (May 21, 2026)
  • Plain-language summary written by qwen3:4b on August 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA