Good Herbs Inc. recalls PRO VITALITY PLUS capsules made on or after October 17, 2013 due to not meeting Good Manufacturing Practices. Consumers should check their product lot dates.
Products not manufactured under GMP's
Good Herbs Inc. is recalling PRO VITALITY PLUS capsules produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This recall is important because products not meeting these standards could pose safety risks.
Products not manufactured under Good Manufacturing Practices (GMPs) may not meet quality and safety standards. This could lead to potential issues with the supplement's purity or effectiveness, though serious injury is not typically associated with this type of recall.
People who bought PRO VITALITY PLUS capsules from Good Herbs Inc. after October 17, 2013 are affected. Those with health conditions requiring supplements may be at slightly higher risk.
Check the product label for the lot date. Products distributed on or after October 17, 2013 are affected. The product is sold by Good Herbs Inc. at their Troy, MI location.
Look for the lot date on the capsule packaging; affected products were distributed on or after October 17, 2013.
The products were not manufactured under Good Manufacturing Practices (GMPs), which are quality and safety standards for food and supplements.
Check the product label for the lot date; affected products were distributed on or after October 17, 2013.
The recall record does not specify a remedy, so contact Good Herbs Inc. for further instructions.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0387-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0387-2015 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.