GM Manufacturing recalls Garcinia Series dietary supplements due to cGMP regulatory violations. Consumers should check purchase dates and contact for details.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling Garcinia Series dietary supplements because they violated cGMP regulations. This means the products may not be safe or effective as intended.
The supplements were made without following proper quality control rules. This could lead to unsafe ingredients or incorrect dosing, but the exact harm isn't specified in the recall.
People who purchased Garcinia Series capsules between April 9 and April 12, 2014 are affected. Those using dietary supplements for health purposes are most at risk.
Check for the product name 'Garcinia Series' and the date range April 9 to April 12, 2014. The recall covers capsules sold during this period.
Look for the purchase date on the capsule packaging to confirm if it falls between April 9 and April 12, 2014.
GM Manufacturing is recalling these supplements due to significant violations of cGMP regulations for dietary supplements.
The recall record does not specify a remedy, so contact GM Manufacturing for further instructions.
The recall mentions cGMP violations, which could affect safety or effectiveness, but the exact risks are not detailed in the record.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2272-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2272-2014 from GM Manufacturing. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
