MyNicNaxs recalls Activity Girl Capsules due to undeclared ingredient N-di-desmethylsibutramine. This unapproved substance poses health risks. Consumers should check their boxes and contact the company.
Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared ingredient: N-di-desmethylsibutramine, an analog of sibutramine
MyNicNaxs is recalling Activity Girl Capsules because they contain an undeclared ingredient that wasn't approved by the FDA. This could lead to health risks since the product was marketed without proper regulatory approval.
The product contains N-di-desmethylsibutramine, an analog of sibutramine, which is not approved by the FDA. This undeclared ingredient could cause health issues when taken without proper regulatory oversight.
Anyone who owns or uses the Activity Girl Capsules from MyNicNaxs. People who have taken the capsules may be at risk due to the undeclared ingredient.
Check for Activity Girl Capsules, 400 mg, 30-count boxes distributed by MyNicNaxs, LLC in Deltona, FL. All lots are affected.
Look for Activity Girl Capsules, 400 mg, 30-count boxes distributed by MyNicNaxs, LLC in Deltona, FL.
The product was marketed without FDA approval and contains an undeclared ingredient, so it is not safe to use.
The recall covers all lots; check your product details and contact MyNicNaxs for further instructions.
The product contains an undeclared ingredient that is not approved by the FDA, which poses health risks.
We’ve drafted a message you can send MyNicNaxs to request your refund or repair — edit it as you like.
Subject: Recall D-1372-2014 — MyNicNaxs MyNicNaxs Hello, I own a MyNicNaxs that is covered by recall D-1372-2014 from MyNicNaxs. 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.
