PlainRecalls
FDA Drug Critical Class I Ongoing

69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC

Reported: July 28, 2021 Initiated: March 29, 2021 #D-0688-2021

Product Description

69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC

Reason for Recall

Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making it an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

Details

Recalling Firm
Nuri Trading LLC
Units Affected
N/A
Distribution
USA Nationwide
Location
Fort Lee, NJ

Frequently Asked Questions

What product was recalled?
69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC. Recalled by Nuri Trading LLC. Units affected: N/A.
Why was this product recalled?
Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making it an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 28, 2021. Severity: Critical. Recall number: D-0688-2021.