Liquid Coffee Inc recalls concentrated coffee in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag due to elevated pH level above 4.6. Consumers should check product dates and contact for details.
The pH level in coffee product was elevated above 4.6.
Liquid Coffee Inc is recalling concentrated coffee products in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag because the pH level is elevated above 4.6. This could pose a risk to consumers, though the specific danger is not clearly described in the recall notice.
The recall states the pH level in the coffee product was elevated above 4.6. However, the recall does not explain how this elevated pH level could cause harm to consumers or what specific health risks it might pose.
Anyone who owns or uses Liquid Coffee Inc's concentrated coffee in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag containers. Those who have purchased the product since production began are most at risk.
Check for concentrated coffee products in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag containers. The product was produced with a date used to track the product.
Look for the production date on the container to determine if the product is within the recall timeframe.
The recall states the pH level in the coffee product was elevated above 4.6, but does not specify the health risk or why it is dangerous.
Check for concentrated coffee in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag containers. The product was produced with a date used to track the product.
The recall does not provide a specific remedy, so contact Liquid Coffee Inc for further instructions.
We’ve drafted a message you can send Liquid Coffee Inc to request your refund or repair — edit it as you like.
Subject: Recall F-1125-2016 — Liquid Coffee Inc Liquid Coffee Inc Hello, I own a Liquid Coffee Inc that is covered by recall F-1125-2016 from Liquid Coffee Inc. 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.
