PremierZEN Gold 7000 capsules (UPC 7 28175 42183 2) were recalled due to being marketed without FDA approval and containing unapproved sildenafil and tadalafil. Consumers should check their boxes for the specific product.
Marketed without an approved NDA/ANDA - Product found to be tainted with Sildenafil and Tadalafil.
PremierZEN Gold 7000 capsules were recalled because they were sold without FDA approval and contain sildenafil and tadalafil. This poses a risk of serious health effects due to unapproved drug ingredients.
The capsules were marketed without FDA approval and contain sildenafil and tadalafil, which are prescription drugs. Using these unapproved drugs could cause serious health issues like heart problems or interactions with other medications.
Anyone who owns or uses PremierZEN Gold 7000 capsules (1-count blister cards in 12-per-box packaging) is affected. People with health conditions or those taking other medications are at higher risk.
Check for the UPC 7 28175 42183 2 on the box. The product is a 1-count blister card packaged in 12 cards per box, distributed by New Premier Group in Los Angeles, CA.
Look for the UPC 7 28175 42183 2 on the box to confirm if you have the recalled product.
The capsules were marketed without FDA approval and contain sildenafil and tadalafil, which are prescription drugs.
The recall record does not specify a remedy, so check the product details to confirm if you have the recalled item.
Yes, using unapproved drugs like sildenafil and tadalafil could cause serious health issues such as heart problems or interactions with other medications.
We’ve drafted a message you can send Miracle 8989 to request your refund or repair — edit it as you like.
Subject: Recall D-0633-2021 — Miracle 8989 Miracle 8989 Hello, I own a Miracle 8989 that is covered by recall D-0633-2021 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.
