Good Herbs Inc. recalls Para Formula capsules made on or after Oct 17, 2013 due to not meeting GMP manufacturing standards. Consumers should check their capsules for the lot date and contact the company for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Para Formula capsules produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices (GMPs). This means the capsules may not be safe or effective as intended.
The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards that ensure products are safe and effective. This could mean the capsules might not work as intended or could be unsafe for consumption.
People who bought Para Formula capsules from Good Herbs Inc. on or after October 17, 2013 are likely affected. Those who have taken the capsules recently may be at slightly higher risk due to potential quality issues.
Check the capsule packaging for the lot date, which should be on or after October 17, 2013. The product is sold by Good Herbs Inc. at their location in Troy, Michigan.
Look for the lot date on the packaging, which should be on or after October 17, 2013.
The capsules were not manufactured under Good Manufacturing Practices (GMPs), which are standards that ensure products are safe and effective.
Check the lot date on the packaging. If it's on or after October 17, 2013, contact Good Herbs Inc. for further instructions.
The recall is due to potential quality issues, but there is no mention of serious injury risks in the official notice.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0371-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0371-2015 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.