Good Herbs Inc. recalls PRO VITALITY capsules made on or after Oct 17, 2013 due to not meeting GMP manufacturing standards. Consumers should check their lot dates.
Products not manufactured under GMP's
Good Herbs Inc. is recalling PRO VITALITY capsules produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices (GMPs). This recall is due to potential quality issues that could affect product safety.
The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards to ensure product safety and quality. This could mean the product may not meet expected safety levels, though the specific risk is not detailed in the recall.
Owners of PRO VITALITY capsules purchased on or after October 17, 2013 from the listed address are affected. Consumers most at risk are those who have taken the capsules without verifying the manufacturing standards.
Check the product label for the address 550 Oliver Dr Troy, MI 48084 and the production date. Products distributed on or after October 17, 2013 are affected.
Look for the production date on the capsule label; affected products were distributed on or after October 17, 2013.
The product was not manufactured under Good Manufacturing Practices (GMPs), which are standards to ensure product safety and quality.
Check the production date on the label; if it's on or after October 17, 2013, contact Good Herbs Inc. for further instructions.
The recall states the product was not made under GMPs, but does not specify a risk of serious injury or harm.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0385-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0385-2015 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.
