Good Herbs Inc. recalls LUNG SUPPORT 2 bottles made on or 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 LUNG SUPPORT 2 herbal bottles made on or after October 17, 2013 because they weren't produced under proper Good Manufacturing Practices. This could mean the products aren't safe or consistent as they should be.
The products weren't made under Good Manufacturing Practices (GMPs), which are standards for food safety and quality. This could lead to inconsistent product quality or safety concerns, but the recall doesn't specify a risk of serious injury or illness.
People who bought Good Herbs LUNG SUPPORT 2 herbal bottles made on or after October 17, 2013. Those using the product for health reasons may be at slightly higher risk due to potential quality issues.
Check for the product name 'LUNG SUPPORT 2' on the bottle. Look for the manufacturing date of October 17, 2013 or later. The product was sold by Good Herbs Inc. in Troy, MI.
Look for the manufacturing date on the bottle label, which should be October 17, 2013 or later.
The recall states the products were not manufactured under Good Manufacturing Practices, but does not specify if they are unsafe. Consumers should check with Good Herbs Inc. for details.
Check the bottle for the product name 'LUNG SUPPORT 2' and a manufacturing date of October 17, 2013 or later.
The recall does not specify a remedy, so contact Good Herbs Inc. directly for guidance.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0333-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0333-2015 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.
