Good Herbs Inc. recalls 4 oz kidney and bladder foundation herbs produced after October 17, 2013 due to failure to meet Good Manufacturing Practices. Consumers should check product lot dates and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling their 4 oz kidney and bladder foundation herbal products made on or after October 17, 2013 because they weren't produced under proper Good Manufacturing Practices. This recall doesn't specify a health risk but indicates potential quality issues with the product.
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 as effective or could have contaminants, but the recall doesn't specify a health hazard.
Anyone who purchased Good Herbs Inc.'s 4 oz kidney and bladder foundation herbal products made on or after October 17, 2013. People using these products for health purposes may be at slightly higher risk due to the quality concerns.
Check for the product name 'Kidney & Bladder Foundation', 4 oz bottle, and the lot date of October 17, 2013 or later. The products were distributed by Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084.
Look for the lot date on the product label to confirm if it was made on or after October 17, 2013.
The recall states the products were not manufactured under Good Manufacturing Practices, but it does not specify a health hazard or injury risk.
Check if your product is labeled 'Kidney & Bladder Foundation', 4 oz bottle, and made on or after October 17, 2013.
The recall does not provide a specific remedy, so contact Good Herbs Inc. directly for further instructions.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0321-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0321-2015 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.
