Multi-event March 2021 FDA Recall Drug by Nuri Trading Llc

This Multi-event Class I drug recall was voluntarily initiated by Nuri Trading Llc on March 29, 2021 for the product Drug. The FDA reported the reason for recall as marketed without an approved nda/anda. The product was distributed Nationwide and the recall is currently ongoing.

Reported Recall Events

Recall Number: D-0685-2021

Reason for Recall
Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.
Initiated
03-29-2021
Reported
07-28-2021
Quantity
N/A

Recall Profile & Regulatory Data

Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Batch or Lot Expiration Information

Lot# all lots within expiry

Recall Number: D-0686-2021

Reason for Recall
Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil, an FDA approved drug making this an unapproved drug for which the safety and efficacy has not been established and therefore subject to recall.
Initiated
03-29-2021
Reported
07-28-2021
Quantity
N/A

Recall Profile & Regulatory Data

Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Batch or Lot Expiration Information

Lot# all lots within expiry

Recall Number: D-0687-2021

Reason for Recall
Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil sildenafil, and vardenafil, FDA approved drugs making them an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.
Initiated
03-29-2021
Reported
07-28-2021
Quantity
N/A

Recall Profile & Regulatory Data

Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Batch or Lot Expiration Information

Lot# all lots within expiry

Recall Number: D-0688-2021

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.
Initiated
03-29-2021
Reported
07-28-2021
Quantity
N/A

Recall Profile & Regulatory Data

Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC

Batch or Lot Expiration Information

Lot# all lots within expiry