Good Herbs Inc. recalls Flower Essence Beech bottles made on or after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check product labels for affected lots.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Flower Essence Beech bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall does not pose a direct health risk but ensures product quality 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 expected quality levels for herbal products, but there is no indication of direct health hazards.
Anyone who owns or uses Good Herbs Flower Essence Beech bottles made on or after October 17, 2013. People using these products for aromatherapy or herbal remedies are most at risk if they have concerns about product quality.
Check for the product name 'Flower Essence Beech' and the lot date of October 17, 2013 or later. The bottles are sold by Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084.
Look for the lot date on the bottle label, which should be October 17, 2013 or later for affected products.
The recall is due to not meeting Good Manufacturing Practices, but there is no indication of direct health risks. The product may not meet quality standards.
Check the bottle label for 'Flower Essence Beech' and a lot date of October 17, 2013 or later.
The recall does not specify a remedy, so no action is required beyond checking the product label.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0207-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0207-2015 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.
