Key Takeaway

69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC by Nuri Trading LLC was recalled on March 29, 2021. The hazard: Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making it an unapp...

FDA Drug Class I Ongoing

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

Recalled: March 29, 2021 ~N/A units affected D-0688-2021

Description

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

Hazard / Reason

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.

Class I: Dangerous or defective product that could cause serious health problems or death.

Class I is the most serious recall classification used by the FDA, indicating a reasonable probability of serious health consequences or death.

Products Affected

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

Drugs

Company Information

Nuri Trading LLC

Fort Lee, NJ, United States

View all 4 recalls by Nuri Trading LLC →

Distribution

USA Nationwide

Related Recalls

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Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

March 29, 2021
FDA Drug Class I

Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

March 29, 2021
FDA Drug Class I

Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

March 29, 2021

Frequently Asked Questions

Is this recall still active?

Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.

How do I check if my product is affected?

Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.

What remedy is available for this recall?

Check the remedy section above or contact the manufacturer directly for current remedy options.

Where can I find the original recall notice?

This recall was issued by FDA Drug. Visit the agency's official website for the original notice.

Data sourced from FDA Drug Enforcement. Recall information may not reflect the most current status. RecallDex is not affiliated with any US government agency. Contact the manufacturer or relevant agency for the latest information.