Good Herbs Inc. recalls Para Formula 3 herbal bottles made on or after October 17, 2013 for not meeting FDA manufacturing standards. Consumers should check product details and contact the company for guidance.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Para Formula 3 herbal bottles produced on or after October 17, 2013 because they were not made under FDA-approved manufacturing practices. This could mean the product may not be safe for consumption.
The product was not manufactured under FDA-approved Good Manufacturing Practices (GMPs), which means it might contain harmful substances or be inconsistent in quality. This could lead to health issues if consumed, though the risk is not severe.
Anyone who purchased Para Formula 3 herbal bottles from Good Herbs Inc. on or after October 17, 2013. People using these products for medicinal purposes may be at slightly higher risk due to potential contamination.
Check for the product name 'Para Formula 3', 4 oz bottle, and the manufacturing date of October 17, 2013 or later. The product was distributed by Good Herbs Inc. at 550 Oliver Dr, Troy, MI 48084.
Look for the product name 'Para Formula 3', 4 oz bottle, and the manufacturing date of October 17, 2013 or later.
The product was not manufactured under FDA-approved Good Manufacturing Practices (GMPs), which could mean it contains harmful substances or is inconsistent in quality.
The recall record does not specify a remedy, so contact Good Herbs Inc. for guidance.
The recall indicates potential safety concerns, but the record does not specify if the product is safe to use.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0374-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0374-2015 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.
