Good Herbs Inc. recalls Mental Alertness 1 oz bottles made on or after Oct 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their bottles for the lot date.
Products not manufactured under GMP's
Good Herbs Inc. is recalling their Mental Alertness herbal supplements made on or after October 17, 2013 because they weren't produced under proper Good Manufacturing Practices. This recall doesn't pose an immediate safety risk but could affect product quality and safety standards.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product quality and safety. This means the supplements might not meet the expected quality and safety standards, but it does not indicate an immediate health hazard.
Anyone who purchased Good Herbs Mental Alertness 1 oz bottles made on or after October 17, 2013. People using these products for mental alertness purposes may be at risk of receiving substandard herbal supplements.
Check for the product name 'Mental Alertness', 1 oz bottle, and the lot date of October 17, 2013 or later. The products were distributed by Good Herbs Inc. from their Troy, MI address.
Look for the lot date on the bottle, which should be October 17, 2013 or later.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are standards for ensuring product quality and safety.
Check for the product name 'Mental Alertness', 1 oz bottle, and the lot date of October 17, 2013 or later.
The recall does not specify a remedy, so no action is required beyond checking if you have the product.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0344-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0344-2015 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.
