Good Herbs Inc. recalls sickle-pod senna products made after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their bottles for the date and take action if affected.
Products not manufactured under GMP's
Good Herbs Inc. is recalling sickle-pod senna products made on or after October 17, 2013 because they were not manufactured under Good Manufacturing Practices. This recall is important because products not meeting these standards could pose safety risks.
Products not manufactured under Good Manufacturing Practices (GMPs) may not meet safety and quality standards. This could lead to potential issues with the product's effectiveness or safety, though the risk is not severe enough to cause serious injury.
Anyone who owns or uses sickle-pod senna products made on or after October 17, 2013. People who use these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for the product name 'Sickle-Pod Senna', 1 oz bottle, and the distribution date of October 17, 2013 or later. The product was distributed by Good Herbs, Inc. from their address in Troy, MI.
Look for the distribution date on the product label, which should be October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could affect their safety and quality.
The recall record does not specify a remedy, so you should check with Good Herbs, Inc. for further instructions.
The recall indicates potential quality issues but does not mention a risk of serious injury, so the danger level is low risk.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0411-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0411-2015 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.
