Good Herbs Inc. recalls scleranthus 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 scleranthus flower essence bottles produced on or after October 17, 2013, because they were not made under Good Manufacturing Practices. This recall does not pose an immediate health risk but ensures product safety standards are met.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This means the bottles might not meet the required quality standards for herbal products, though the recall does not indicate a specific health hazard.
Anyone who purchased Good Herbs Inc.'s scleranthus flower essence bottles from October 17, 2013, onward. People using these products for aromatherapy or herbal remedies are most at risk if the product was not manufactured under proper quality controls.
Check for the product name 'Scleranthus Flower Essence' in 1 or 4 oz bottles with the address 550 Oliver Dr, Troy, MI 48084. The recall applies to all lots distributed on or after October 17, 2013.
Look for the distribution date on the bottle, which must be on or after October 17, 2013.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality.
The recall does not specify a remedy, so contact Good Herbs Inc. for further instructions.
The recall does not indicate a specific health hazard, so the risk is considered low.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0233-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0233-2015 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.
