Schindele Enterprises recalls XZONE GOLD 750mg capsules due to undeclared sildenafil and tadalafil. These supplements may contain unsafe levels of these drugs without FDA approval.
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Schindele Enterprises is recalling XZONE GOLD 750mg dietary supplements because they contain undeclared sildenafil and tadalafil without FDA approval. This poses a risk of serious health effects due to the unapproved drugs.
These supplements contain undeclared sildenafil and tadalafil, which are prescription drugs. Without FDA approval, they may cause serious health issues like heart problems or interactions with other medications.
People who purchased XZONE GOLD 750mg capsules from XZONE in Orlando, Florida. Those with heart conditions or who take medications that interact with sildenafil or tadalafil are at higher risk.
Check for XZONE GOLD 1 capsule blister packs labeled 750 mg. The lot number 130710GL was distributed by XZONE in Orlando, Florida with an expiration date of 07/31/2018.
Look for the lot number 130710GL on the packaging to confirm if your XZONE GOLD 750mg capsules are affected.
The product contains undeclared sildenafil and tadalafil without FDA approval, which can cause serious health issues.
The recall record does not specify a remedy, so check the product details to confirm if it's affected and contact the manufacturer for further instructions.
No, the product contains undeclared prescription drugs without FDA approval, which may cause serious health risks.
We’ve drafted a message you can send Schindele Enterprises to request your refund or repair — edit it as you like.
Subject: Recall D-1334-2014 — Schindele Enterprises Schindele Enterprises Hello, I own a Schindele Enterprises that is covered by recall D-1334-2014 from Schindele Enterprises. 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.
