Good Herbs Inc. recalls BLADDERWRACK herbs from 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 BLADDERWRACK herbal products sold in 1 and 4 oz bottles from October 17, 2013, because they were not made under Good Manufacturing Practices. This could mean the products are unsafe for consumption.
Products not manufactured under Good Manufacturing Practices (GMPs) may have contaminants or quality issues that could affect safety. This is a regulatory compliance issue rather than an immediate physical hazard.
Anyone who purchased Good Herbs BLADDERWRACK herbal products from October 17, 2013, onward. People using these products for medicinal purposes may be at slightly higher risk due to potential contamination.
Check for the product name 'BLADDERWRACK' in 1 or 4 oz bottles. Look for the 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 product label, which should be October 17, 2013 or later.
Reach out to Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084 for further assistance.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could lead to potential contamination or quality issues.
Check the distribution date on the label. If it's October 17, 2013 or later, contact Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084 for further instructions.
The recall is due to potential contamination or quality issues, not an immediate physical hazard like a fire or injury. 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-0124-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0124-2015 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.