FDAClass IIMay 26, 2021

Triple SupremeZen Plus 3500 recall

Triple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ

Why was Triple SupremeZen Plus 3500 recalled?

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

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 lots

Product
Triple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ
Recalling firm
Hyobin LLC
Quantity
300 cards
Distribution
USA Nationwide
Recall date
May 26, 2021
Classification
Class II
Status
Ongoing
Agency
FDA (drug)
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