Good Herbs Inc. recalls Performance Plus capsules made on or after Oct 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their capsules for the lot date.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Performance Plus capsules produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could mean the capsules are unsafe for consumption.
The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards for food safety. This could mean the capsules might not be safe to consume, but the recall does not specify a risk of serious injury.
People who bought Performance Plus capsules from Good Herbs Inc. after October 17, 2013. Those who have already taken the capsules may not be at immediate risk.
Check the product label for the lot date. The capsules were distributed on or after October 17, 2013. The product name is Performance Plus capsules from Good Herbs Inc.
Look for the lot date on the capsule packaging to determine if it falls within the recall range (October 17, 2013 or later).
The recall states the capsules were not manufactured under Good Manufacturing Practices, but it does not specify that they are unsafe. Consumers should check the lot date and follow the recall instructions.
The recall does not provide a specific remedy, so you should check the lot date and contact Good Herbs Inc. if you have capsules made on or after October 17, 2013.
Check the product label for the lot date. The recalled capsules were distributed on or after October 17, 2013, and are labeled as Performance Plus capsules from Good Herbs Inc.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0379-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0379-2015 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.
