Good Herbs Inc. recalls Spirulina capsules made on or after Oct 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check product lot dates.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Spirulina capsules produced on or after October 17, 2013 because they were not manufactured under Good Manufacturing Practices. This could mean the products may not be safe or effective.
The capsules were not made under Good Manufacturing Practices, which means they might not be safe or effective. This could lead to health issues if the product is contaminated or not properly processed.
People who bought Good Herbs Spirulina capsules made on or after October 17, 2013. Those who have taken these capsules are most at risk.
Check the product label for the manufacturer's address: 550 Oliver Dr Troy, MI 48084. Look for the production date on or after October 17, 2013.
Look for the production date on the capsule label, which should be on or after October 17, 2013.
The capsules were not manufactured under Good Manufacturing Practices, which could mean they are unsafe or ineffective.
Check the product label for the manufacturer's address: 550 Oliver Dr Troy, MI 48084, and the production date on or after October 17, 2013.
The recall record does not specify a remedy, so there is no action required beyond checking the product date.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0419-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0419-2015 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.