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Miracle8989 Supplement - recalled due to undeclared sildenafil and tadalafil, USA

2 years ago

United States

Company name: Miracle8989
Brand name: PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000 capsules
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: May 19, 2021
Recall details: Irving, Texas, Miracle8989 is voluntarily recalling all lots PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000, capsules to the consumer level. FDA analysis has found the products to contain undeclared sildenafil and tadalafil.  Sildenafil and Tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction.  The presence of Sildenafil and Tadalafil in PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000 renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall.

Risk Statement: Consumers with underlying medical issues who take PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000 with undeclared Sildenafil and Tadalafil may experience serious health risks.  For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening.  Consumers with diabetes, high blood pressure, or heart disease often take nitrates.

To date, Ebay Seller Annie Cho has not received any reports of adverse events related to this recall.

The tainted PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000 products are marketed as dietary supplements for male sexual enhancement and is packaged in 1 count blister cards. The affected PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000 include all lot numbers and all expiration dates. The product can be identified by the product name and the UPC codes below distributed nationwide via internet.

Product Name UPC codes
PremierZen Gold 7000 728175421832
PremierZen Platinum 8000 728175421832
MaxxZEN Platinum 12000 718122040728

Miracle8989 is notifying its distributors and customers by sending eBay messages and is arranging for return of all recalled products. Consumers that have PremierZen Gold 7000, PremierZen Platinum 8000, and MaxxZEN Platinum 12000 which is being recalled should stop using.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax.

Check the full recall details on fda.gov

Source: FDA

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Company name: Backstage Center
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San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native... See More to Mexico and Central America. H&NATURAL TejoRoot and H&NATURAL Brazil Seed were distributed Nationwide to via internet on their site, Amazon.com, and Walmart.com. The company has received one report of gastrointestinal illness, including painful symptoms in conjunction with internal bleeding in connection with H&NATURAL TejoRoot, and has not received any reports of adverse events in connection with H&NATURAL Brazil Seed.

Risk Statement: Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

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Company name: Nordic Naturals
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