GM Manufacturing recalls DMSA dietary supplements in 100cc HDPE bottles (LOTKZ801:10.2016) due to cGMP regulatory violations. Consumers should contact the company for details.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling dietary supplements in 100cc HDPE bottles because they violated food safety regulations. This could pose risks to consumers using these products.
The product was made in violation of current Good Manufacturing Practices (cGMP) for dietary supplements. This means the supplements may not be safe or effective, potentially causing harm to consumers.
Dietary supplement users who purchased the DMSA 100cc HDPE bottles with lot number LOTKZ8010 (expired 10.2016) are affected. Those using these products without proper quality control are at higher risk.
Check for the product name 'DMSA', 100cc HDPE bottle, and lot number LOTKZ8010 (expired 10.2016). The product was sold in the U.S. market.
Reach out to GM Manufacturing Inc. for specific instructions on handling the recalled product.
The product was made in violation of current Good Manufacturing Practices (cGMP) for dietary supplements.
Contact GM Manufacturing Inc. for specific instructions on handling the recalled product.
The recall is due to regulatory violations, but the official notice does not specify injury risks.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2266-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2266-2014 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.
