Regeneca Worldwide recalls all RegeneFit dietary supplements due to failure to meet current Good Manufacturing Practice regulations for dietary supplements. Consumers should check lot numbers for affected products.
The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
Regeneca Worldwide is recalling all Regene:Fit dietary supplements because they were not made according to current dietary supplement manufacturing standards. This recall is important because products not meeting these standards could pose safety risks.
The supplements were not manufactured in compliance with current Good Manufacturing Practice regulations for dietary supplements. This means the products may not meet safety and quality standards required by law, potentially leading to health risks.
Dietary supplement users who purchased RegeneFit products with lot number B1109329 are affected. Those most at risk are individuals who consume supplements regularly without checking manufacturing compliance.
Check the lot number on the product label, which should be B1109329 for affected RegeneFit supplements. The product name is RegeneFit and the manufacturer is VivaCeuticals, Inc. dba Regeneca Worldwide.
Look for the lot number B1109329 on the RegeneFit supplement label.
Regeneca Worldwide is recalling all RegeneFit dietary supplements because they were not manufactured in compliance with current Good Manufacturing Practice regulations for dietary supplements.
Check the lot number on the product label. If it is B1109329, contact Regeneca Worldwide for instructions.
The recall is due to manufacturing compliance issues, but the official notice does not specify a risk of serious injury or death. The danger level is low risk.
We’ve drafted a message you can send Regeneca Worldwide to request your refund or repair — edit it as you like.
Subject: Recall F-1825-2017 — Regeneca Worldwide Regeneca Worldwide Hello, I own a Regeneca Worldwide that is covered by recall F-1825-2017 from Regeneca Worldwide. 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.
