FDAClass IIMay 12, 2021

PremierZen Extreme 3000 recall

PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887

Why was PremierZen Extreme 3000 recalled?

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

All

Product
PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887
Recalling firm
QMart
Quantity
500 boxes
Distribution
USA Nationwide
Recall date
May 12, 2021
Classification
Class II
Status
Ongoing
Agency
FDA (drug)
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