Good Herbs Inc. recalls 1oz Shepherd's Purse bottles from October 17, 2013 onward due to not meeting Good Manufacturing Practices. Consumers should check product details and contact the company for guidance.
Products not manufactured under GMP's
Good Herbs Inc. is recalling 1-ounce Shepherd's Purse bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall is due to potential quality issues that could affect product safety.
Products not manufactured under Good Manufacturing Practices (GMPs) may have quality issues that could affect safety. This means the herbs might not meet the required standards for purity and consistency, potentially leading to adverse effects if used improperly.
Anyone who owns or uses Good Herbs Inc.'s 1-ounce Shepherd's Purse bottles purchased on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to quality concerns.
Check for the product name 'Shepherd's Purse', 1-ounce bottle, and 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 product name 'Shepherd's Purse', 1-ounce bottle, and distribution date of October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which could lead to quality issues affecting safety.
The recall record does not specify a remedy, so contact Good Herbs Inc. for guidance.
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-0409-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0409-2015 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.
