FDAClass IOctober 26, 2016

Ninja-X recall

Ninja-X, 4200 mg, 1 capsule per pack, 24 single packs per box.

Why was Ninja-X recalled?

Marketed without an approved NDA/ANDA: FDA sample analyses revealed the presence of undeclared sildenafil and/or its analogs in products marketed as dietary supplements

What should I do if I have this product?

Review the official FDA enforcement record for current 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: 7920888; Best Use by: 6/31/2018

Product
Ninja-X, 4200 mg, 1 capsule per pack, 24 single packs per box.
Recalling firm
SOS Telecom Inc.
Quantity
N/A
Distribution
NY
Recall date
October 26, 2016
Classification
Class I
Status
Terminated
Agency
FDA (drug)
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