Miracle 8989 recalls maXXzen Platinum 12000 capsules (UPC 7 18122 04072 8) distributed by Maxx Inc. The product was found to contain unapproved sildenafil and tadalafil, posing a safety risk.
Marketed without an approved NDA/ANDA - Product found to be tainted with Sildenafil and Tadalafil.
Miracle 8989 has recalled maXXzen Platinum 12000 capsules (1-count blister card) due to being found to contain unapproved sildenafil and tadalafil. This poses a safety risk as the product was marketed without an approved drug application.
The product was marketed without an approved drug application (NDA/ANDA) and was found to contain sildenafil and tadalafil, which are prescription medications. This means the product could cause unintended health effects if taken without proper medical supervision.
People who purchased the maXXzen Platinum 12000 capsules (UPC 7 18122 04072 8) from Maxx Inc. in Los Angeles, CA are affected. Those who have taken the product without knowing it contains unapproved medications are at risk.
Check for the maXXzen Platinum 12000 capsule (1-count blister card) with UPC 7 18122 04072 8. The product was distributed by Maxx Inc. in Los Angeles, CA.
Identify the product by UPC 7 18122 04072 8 or the maXXzen Platinum 12000 capsule (1-count blister card) label.
The product was found to contain unapproved sildenafil and tadalafil and was marketed without an approved drug application (NDA/ANDA).
The recall record does not specify a remedy, so check the product details and contact the manufacturer for further instructions.
The recall record does not describe specific injury risks, so the danger level is unknown.
We’ve drafted a message you can send Miracle 8989 to request your refund or repair — edit it as you like.
Subject: Recall D-0635-2021 — Miracle 8989 Miracle 8989 Hello, I own a Miracle 8989 that is covered by recall D-0635-2021 from Miracle 8989. 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.
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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.
