FDA recall record

Nuri Trading 69MODE Blue 69 capsule recall — FDA D-0688-2021

Marketed Without An Approved NDA/ANDA: Product found to be tainted with undeclared tadalafil and sildenafil, two FDA approved drugs making it an…

Class Iclassification
D-0688-2021official record ID
Jul 28, 2021report date

Recall record at a glance

Official recordD-0688-2021
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmNuri Trading LLC
Report dateJul 28, 2021
Recall initiation dateMar 29, 2021
QuantityN/A
LocationFort Lee, NJ, United States

Official product description

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

Why the product was 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.

Distribution information

USA Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.