Red Diamond recalls European Roast Coffee Concentrate with elevated pH levels that could cause safety issues. Learn if you have the affected product and what to do.
Elevated pH levels in an acidified product
Red Diamond is recalling a specific coffee concentrate product due to elevated pH levels in the acidified product. This could pose safety risks if the product is used improperly.
The coffee concentrate has elevated pH levels in an acidified product, which could lead to safety concerns if the product is not handled correctly. This pH imbalance might affect the product's stability and safety.
Coffee drinkers who purchased the specific Red Diamond European Roast Coffee Concentrate product from the listed manufacturer. Those using the product for regular consumption are most at risk.
Check for the product name 'Red Diamond, European Roast, Coffee Concentrate', mix ratio 69 + 1, and net contents 1/2 gallon. The item number is 111590, and it was manufactured for Red Diamond in Birmingham, AL.
Look for the product name, mix ratio, net contents, item number, and manufacturing location on the label.
The recall states elevated pH levels in the acidified product, but does not specify if it is safe to use. The official notice does not provide details on safety.
The recall remedy is not stated, so there is no specific action required. Check the product details to confirm if it is affected.
Check for the product name 'Red Diamond, European Roast, Coffee Concentrate', mix ratio 69 + 1, net contents 1/2 gallon, item number 111590, and manufacturing location in Birmingham, AL.
We’ve drafted a message you can send Red Diamond to request your refund or repair — edit it as you like.
Subject: Recall F-0619-2016 — Red Diamond Red Diamond Hello, I own a Red Diamond that is covered by recall F-0619-2016 from Red Diamond. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.