Good Herbs Inc. recalls Schisandra herbal supplements made after 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 Schisandra herbal supplements produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall does not pose an immediate safety risk but is important for quality assurance.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product quality and safety. This means the supplements may not meet the expected quality levels, but the recall does not indicate a risk of injury or illness.
People who purchased Good Herbs Schisandra herbal supplements from stores or online after October 17, 2013 are affected. Those who have the product are most at risk if they use it without knowing the recall.
Check for the product name 'Schisandra', 4 oz 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 distribution date on the label, which should be October 17, 2013 or later.
Reach out to Good Herbs Inc. for further information about the recall and any necessary actions.
No, the recall is due to not meeting Good Manufacturing Practices, which does not pose a risk of injury or illness. The product is safe to use but should be returned as part of the recall.
The product was distributed on or after October 17, 2013.
The official recall notice does not specify refunds or replacements; contact Good Herbs Inc. directly for details.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0406-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0406-2015 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.
