Good Herbs Inc. recalls LINDEN 1 & 4 oz herb bottles made on or after October 17, 2013 due to failure to meet Good Manufacturing Practices. Consumers should check product labels for affected lots.
Products not manufactured under GMP's
Good Herbs Inc. is recalling LINDEN 1 and 4 oz herb bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could mean the products do not meet safety and quality standards, though no specific harm has been reported.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product safety and quality. This could mean the herbs might not be properly processed or stored, potentially leading to contamination or inconsistent potency. However, no specific injuries or illnesses have been reported from these products.
Anyone who owns or uses Good Herbs LINDEN 1 & 4 oz bottles purchased on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to potential quality issues.
Check for the product name 'LINDEN' and sizes 1 or 4 oz on the bottle. The recall applies to bottles distributed on or after October 17, 2013, with the address 550 Oliver Dr, Troy, MI 48084.
Look for the product name 'LINDEN' and sizes 1 or 4 oz on the bottle.
The recall record does not mention any injuries or illnesses associated with these products.
The recall record does not specify a remedy, so no action is required beyond checking the product label.
The products were distributed on or after October 17, 2013.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0328-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0328-2015 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.