NUX Male Enhancement capsule recall
NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
Why was NUX Male Enhancement capsule recalled?
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
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?
Lot#: RO 927996, Exp: 12/25/2024
- Product
- NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
- Recalling firm
- Gadget Island, Inc
- Quantity
- 18 blister cards
- Distribution
- Nationwide in the USA.
- Recall date
- May 10, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)