Good Herbs Inc. recalls Japanese Honeysuckle & Forsythia products made after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check product dates and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Japanese Honeysuckle and Forsythia herbal products made on or after October 17, 2013 because they were not manufactured under Good Manufacturing Practices. This could lead to unsafe products that don't meet quality standards.
Products not made under Good Manufacturing Practices (GMPs) may not meet safety and quality standards. This could result in products that are unsafe for consumption, though the specific risks are not detailed in the recall notice.
Anyone who owns or uses Good Herbs Japanese Honeysuckle or Forsythia products purchased on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for the product name 'Japanese Honeysuckle & Forsythia' on the label. Look for the bottle size (1 or 4 oz) and the distribution date of October 17, 2013 or later.
Look for the distribution date on the label; products made on or after October 17, 2013 are affected.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could affect their safety and quality.
The recall notice does not specify a remedy, so contact Good Herbs Inc. directly for further instructions.
The recall states products were not made under GMPs, but specific safety risks are not detailed in the notice.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0312-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0312-2015 from Good Herbs. 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.
