Good Herbs Inc. recalls honeysuckle flower essence bottles from October 2013 due to failure to meet 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 honeysuckle flower essence bottles produced on or after October 17, 2013, because they weren't made under proper Good Manufacturing Practices. This could mean the products aren't safe or reliable for use.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety and quality. This could lead to inconsistent quality or safety issues, but the recall doesn't specify a direct health risk like illness or injury.
People who bought Good Herbs honeysuckle flower essence bottles from October 17, 2013, onward. Those using the product for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for bottles labeled 'Good Herbs, Inc., FLOWER ESSENCE HONEYSUCKLE, 1 & 4 oz' with a distribution date of October 17, 2013 or later. The product was sold by Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084.
Look for the distribution date on the bottle, which should be October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety and quality.
Check for bottles labeled 'Good Herbs, Inc., FLOWER ESSENCE HONEYSUCKLE, 1 & 4 oz' with a distribution date of October 17, 2013 or later.
The recall record does not specify a remedy, so contact Good Herbs Inc. for further instructions.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0221-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0221-2015 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.
