US Drug Recall Register
Class I · High risk Terminated Initiated May 12, 2016 (10 years ago)

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

Class I — High risk. Reasonable probability of serious harm or death.

Why it was 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 was recalled

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

Recalling firm
SOS Telecom Inc.
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0102-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.